Linked Data
ClinVar Variation Id:
525390
dbSNP Id:
rs1193586811
gnomAD v2:
5-13792147-G-A
gnomAD v3:
5-13792038-G-A
gnomAD v4:
5-13792038-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.13792038G>A , CM000667.2:g.13792038G>A | GRCh38 |
| NC_000005.9:g.13792147G>A , CM000667.1:g.13792147G>A | GRCh37 |
| NC_000005.8:g.13845147G>A | NCBI36 |
| NG_013081.1:g.157443C>T | |
| NG_013081.2:g.157443C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265104.5:c.8404C>T MANE Select | ENSP00000265104.4:p.Gln2802Ter | |
| ENST00000681290.1:c.8359C>T | ENSP00000505288.1:p.Gln2787Ter | |
| ENST00000265104.4:c.8404C>T | ENSP00000265104.4:p.Gln2802Ter | |
| NM_001369.2:c.8404C>T | NP_001360.1:p.Gln2802Ter | |
| XM_005248262.2:c.8359C>T | XP_005248319.1:p.Gln2787Ter | |
| XM_011513990.1:c.8404C>T | XP_011512292.1:p.Gln2802Ter | |
| XR_925598.1:n.8611C>T | ||
| XM_005248262.3:c.8512C>T | XP_005248319.2:p.Gln2838Ter | |
| XM_017009177.1:c.8512C>T | XP_016864666.1:p.Gln2838Ter | |
| XM_017009178.1:c.7417C>T | XP_016864667.1:p.Gln2473Ter | |
| XM_017009179.2:c.7417C>T | XP_016864668.1:p.Gln2473Ter | |
| XM_017009180.1:c.8512C>T | XP_016864669.1:p.Gln2838Ter | |
| XM_017009181.1:c.8512C>T | XP_016864670.1:p.Gln2838Ter | |
| XM_017009182.1:c.8512C>T | XP_016864671.1:p.Gln2838Ter | |
| XM_017009183.1:c.8512C>T | XP_016864672.1:p.Gln2838Ter | |
| XM_017009184.1:c.8512C>T | XP_016864673.1:p.Gln2838Ter | |
| XM_017009185.1:c.3601C>T | XP_016864674.1:p.Gln1201Ter | |
| XM_017009186.1:c.3154C>T | XP_016864675.1:p.Gln1052Ter | |
| XM_017009188.1:c.2491C>T | XP_016864677.1:p.Gln831Ter | |
| XM_024454388.1:c.7417C>T | XP_024310156.1:p.Gln2473Ter | |
| XM_024454389.1:c.7006C>T | XP_024310157.1:p.Gln2336Ter | |
| XR_001742034.1:n.8529C>T | ||
| XR_001742035.1:n.8529C>T | ||
| NM_001369.3:c.8404C>T MANE Select | NP_001360.1:p.Gln2802Ter |