Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.21880719C>A , CM000669.2:g.21880719C>A | GRCh38 |
| NC_000007.13:g.21920337C>A , CM000669.1:g.21920337C>A | GRCh37 |
| NC_000007.12:g.21886862C>A | NCBI36 |
| NG_012886.2:g.342505C>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001277115.2:c.12213C>A MANE Select | NP_001264044.1:p.Cys4071Ter |
| ENST00000409508.8:c.12213C>A MANE Select | ENSP00000475939.1:p.Cys4071Ter |
| NM_001277115.1:c.12213C>A | NP_001264044.1:p.Cys4071Ter |
| ENST00000328843.10:c.12234C>A | ENSP00000330671.7:p.Cys4078Ter |
| ENST00000409508.7:c.12213C>A | ENSP00000475939.1:p.Cys4071Ter |
| ENST00000620169.4:c.12234C>A | ENSP00000481693.1:p.Cys4078Ter |