Linked Data
dbSNP Id:
rs2803085
gnomAD v2:
6-163142618-A-C
gnomAD v3:
6-162721586-A-C
gnomAD v4:
6-162721586-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.162721586A>C , CM000668.2:g.162721586A>C | GRCh38 |
| NC_000006.11:g.163142618A>C , CM000668.1:g.163142618A>C | GRCh37 |
| NC_000006.10:g.163062608A>C | NCBI36 |
| NG_008289.1:g.11217T>G | |
| NG_008289.2:g.11217T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000338468.8:c.7+6076T>G | ENSP00000343589.4:n.7+6076T>G | |
| ENST00000366894.6:c.7+6076T>G | ENSP00000355860.2:n.7+6076T>G | |
| ENST00000366898.6:c.7+6076T>G MANE Select | ENSP00000355865.1:n.7+6076T>G | |
| ENST00000642604.1:n.25+6076T>G | ||
| ENST00000647006.2:c.-214+6076T>G | ENSP00000501337.1:n.-214+6076T>G | |
| ENST00000674176.1:n.25+6076T>G | ||
| ENST00000674224.1:n.25+6076T>G | ||
| ENST00000674232.1:n.25+6076T>G | ||
| ENST00000674250.1:c.7+6076T>G | ENSP00000501354.1:n.7+6076T>G | |
| ENST00000674353.1:n.24+6076T>G | ||
| ENST00000674395.1:n.25+6076T>G | ||
| ENST00000674493.1:n.24+6076T>G | ||
| ENST00000674501.1:n.114+6076T>G | ||
| ENST00000338468.7:c.-445+6076T>G | ENSP00000343589.3:n.-445+6076T>G | |
| ENST00000366892.5:c.7+6076T>G | ENSP00000355858.1:n.7+6076T>G | |
| ENST00000366894.5:c.-326+6076T>G | ENSP00000355860.1:n.-326+6076T>G | |
| ENST00000366896.5:c.7+6076T>G | ENSP00000355862.1:n.7+6076T>G | |
| ENST00000366897.5:c.7+6076T>G | ENSP00000355863.1:n.7+6076T>G | |
| ENST00000366898.5:c.7+6076T>G | ENSP00000355865.1:n.7+6076T>G | |
| ENST00000479615.5:c.-67+6076T>G | ENSP00000434414.1:n.-67+6076T>G | |
| NM_004562.2:c.7+6076T>G | NP_004553.2:n.7+6076T>G | |
| NM_013987.2:c.7+6076T>G | NP_054642.2:n.7+6076T>G | |
| NM_013988.2:c.7+6076T>G | NP_054643.2:n.7+6076T>G | |
| XM_011535863.1:c.7+6076T>G | XP_011534165.1:n.7+6076T>G | |
| XM_011535864.1:c.7+6076T>G | XP_011534166.1:n.7+6076T>G | |
| XM_011535865.1:c.7+6076T>G | XP_011534167.1:n.7+6076T>G | |
| XM_011535866.1:c.7+6076T>G | XP_011534168.1:n.7+6076T>G | |
| XM_011535867.1:c.7+6076T>G | XP_011534169.1:n.7+6076T>G | |
| XM_017010909.2:c.-67+6076T>G | XP_016866398.1:n.-67+6076T>G | |
| XM_024446449.1:c.-67+6076T>G | XP_024302217.1:n.-67+6076T>G | |
| XR_001743443.2:n.113+6076T>G | ||
| NM_004562.3:c.7+6076T>G MANE Select | NP_004553.2:n.7+6076T>G | |
| NM_013987.3:c.7+6076T>G | NP_054642.2:n.7+6076T>G | |
| NM_013988.3:c.7+6076T>G | NP_054643.2:n.7+6076T>G |