Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.14139290C= , CM000665.2:g.14139290C= | GRCh38 |
| NC_000003.11:g.14180790C= , CM000665.1:g.14180790C= | GRCh37 |
| NC_000003.10:g.14155791C= | NCBI36 |
| NG_008975.1:g.19351C= , LRG_435:g.19351C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000432444.2:c.*1023C= | ENSP00000395617.1:n.*1023C= | |
| ENST00000306077.5:c.993C= MANE Select | ENSP00000303992.5:p.Tyr331= | |
| ENST00000306077.4:c.993C= | ENSP00000303992.4:p.Tyr331= | |
| ENST00000601399.3:n.320C= | ||
| ENST00000608606.1:c.229C= | ||
| NM_024334.2:c.993C= , LRG_435t1:c.993C= | NP_077310.1:p.Tyr331= | |
| XM_011534109.1:c.888C= | XP_011532411.1:p.Tyr296= | |
| XM_017007176.2:c.888C= | XP_016862665.1:p.Tyr296= | |
| NM_024334.3:c.993C= MANE Select | NP_077310.1:p.Tyr331= |