Linked Data
dbSNP Id:
rs1006498585
gnomAD v2:
4-9968627-A-G
gnomAD v3:
4-9967003-A-G
gnomAD v4:
4-9967003-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.9967003A>G , CM000666.2:g.9967003A>G | GRCh38 |
| NC_000004.11:g.9968627A>G , CM000666.1:g.9968627A>G | GRCh37 |
| NC_000004.10:g.9577725A>G | NCBI36 |
| NG_011540.1:g.78246T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264784.8:c.681+13589T>C MANE Select | ENSP00000264784.3:n.681+13589T>C | |
| ENST00000264784.7:c.681+13589T>C | ENSP00000264784.3:n.681+13589T>C | |
| ENST00000309065.7:c.594+13589T>C | ENSP00000311383.3:n.594+13589T>C | |
| ENST00000505104.5:n.715+13589T>C | ||
| ENST00000506583.5:c.594+13589T>C | ENSP00000422209.1:n.594+13589T>C | |
| NM_001001290.1:c.594+13589T>C | NP_001001290.1:n.594+13589T>C | |
| NM_020041.2:c.681+13589T>C | NP_064425.2:n.681+13589T>C | |
| XM_006713968.2:c.681+13589T>C | XP_006714031.1:n.681+13589T>C | |
| XM_006713969.2:c.594+13589T>C | XP_006714032.1:n.594+13589T>C | |
| XM_011513856.1:c.681+13589T>C | XP_011512158.1:n.681+13589T>C | |
| XM_011513857.1:c.594+13589T>C | XP_011512159.1:n.594+13589T>C | |
| XM_011513858.1:c.594+13589T>C | XP_011512160.1:n.594+13589T>C | |
| XM_011513859.1:c.681+13589T>C | XP_011512161.1:n.681+13589T>C | |
| XM_011513860.1:c.681+13589T>C | XP_011512162.1:n.681+13589T>C | |
| XM_011513861.1:c.681+13589T>C | XP_011512163.1:n.681+13589T>C | |
| XM_011513862.1:c.285+13589T>C | XP_011512164.1:n.285+13589T>C | |
| XM_011513863.1:c.285+13589T>C | XP_011512165.1:n.285+13589T>C | |
| XM_011513864.1:c.273+13589T>C | XP_011512166.1:n.273+13589T>C | |
| XM_011513865.1:c.681+13589T>C | XP_011512167.1:n.681+13589T>C | |
| XM_011513866.1:c.681+13589T>C | XP_011512168.1:n.681+13589T>C | |
| XM_011513867.1:c.123+13589T>C | XP_011512169.1:n.123+13589T>C | |
| XM_011513868.1:c.681+13589T>C | XP_011512170.1:n.681+13589T>C | |
| XR_925341.1:n.777+13589T>C | ||
| XM_006713968.4:c.681+13589T>C | XP_006714031.1:n.681+13589T>C | |
| XM_011513856.3:c.681+13589T>C | XP_011512158.1:n.681+13589T>C | |
| XM_011513859.3:c.681+13589T>C | XP_011512161.1:n.681+13589T>C | |
| XM_011513860.3:c.681+13589T>C | XP_011512162.1:n.681+13589T>C | |
| XM_011513861.3:c.681+13589T>C | XP_011512163.1:n.681+13589T>C | |
| XM_011513862.3:c.285+13589T>C | XP_011512164.1:n.285+13589T>C | |
| XM_011513864.2:c.273+13589T>C | XP_011512166.1:n.273+13589T>C | |
| XM_011513865.2:c.681+13589T>C | XP_011512167.1:n.681+13589T>C | |
| XM_011513866.2:c.681+13589T>C | XP_011512168.1:n.681+13589T>C | |
| XM_011513867.3:c.123+13589T>C | XP_011512169.1:n.123+13589T>C | |
| XM_011513868.2:c.681+13589T>C | XP_011512170.1:n.681+13589T>C | |
| XM_017008457.2:c.681+13589T>C | XP_016863946.1:n.681+13589T>C | |
| XM_017008458.2:c.681+13589T>C | XP_016863947.1:n.681+13589T>C | |
| XM_017008459.1:c.219+13589T>C | XP_016863948.1:n.219+13589T>C | |
| XM_017008460.2:c.285+13589T>C | XP_016863949.1:n.285+13589T>C | |
| XM_024454150.1:c.681+13589T>C | XP_024309918.1:n.681+13589T>C | |
| XM_024454151.1:c.294+13589T>C | XP_024309919.1:n.294+13589T>C | |
| XM_024454152.1:c.681+13589T>C | XP_024309920.1:n.681+13589T>C | |
| XM_024454153.1:c.681+13589T>C | XP_024309921.1:n.681+13589T>C | |
| XR_001741290.1:n.854+13589T>C | ||
| XR_001741291.1:n.854+13589T>C | ||
| XR_925341.3:n.858+13589T>C | ||
| NM_020041.3:c.681+13589T>C MANE Select | NP_064425.2:n.681+13589T>C | |
| NM_001001290.2:c.594+13589T>C | NP_001001290.1:n.594+13589T>C |