Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.184135385G= , CM000665.2:g.184135385G= | GRCh38 |
| NC_000003.11:g.183853173G= , CM000665.1:g.183853173G= | GRCh37 |
| NC_000003.10:g.185335867G= | NCBI36 |
| NG_015826.1:g.5364G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000432569.2:c.-1G= | ENSP00000414775.1:n.-1G= | |
| ENST00000465218.3:n.23G= | ||
| ENST00000471832.2:c.-1G= | ENSP00000497786.1:n.-1G= | |
| ENST00000647636.1:c.-1G= | ENSP00000497505.1:n.-1G= | |
| ENST00000647909.1:c.-1G= | ENSP00000498164.1:n.-1G= | |
| ENST00000648314.1:c.-1G= | ENSP00000496920.1:n.-1G= | |
| ENST00000648599.1:c.-1G= | ENSP00000497159.1:n.-1G= | |
| ENST00000648682.1:c.-1G= | ENSP00000498185.1:n.-1G= | |
| ENST00000648882.1:c.-1G= | ENSP00000497603.1:n.-1G= | |
| ENST00000648890.1:c.-1G= | ENSP00000497503.1:n.-1G= | |
| ENST00000648915.2:c.-1G= MANE Select | ENSP00000497160.1:n.-1G= | |
| ENST00000649688.1:c.-1G= | ENSP00000497097.1:n.-1G= | |
| ENST00000649814.1:n.49G= | ||
| ENST00000273783.7:c.-1G= | ENSP00000273783.3:n.-1G= | |
| ENST00000432569.1:c.-1G= | ENSP00000414775.1:n.-1G= | |
| ENST00000444495.1:c.-1G= | ENSP00000409142.1:n.-1G= | |
| ENST00000481054.5:n.1G= | ||
| ENST00000491144.5:n.348G= | ||
| NM_003907.2:c.-1G= | NP_003898.2:n.-1G= | |
| XR_924208.1:n.951G= | ||
| NM_003907.3:c.-1G= MANE Select | NP_003898.2:n.-1G= | |
| XM_011513266.3:c.-902G= | XP_011511568.1:n.-902G= | |
| XR_001740352.2:n.363G= | ||
| XR_001740353.2:n.363G= | ||
| XR_924208.2:n.363G= |