Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48463741G= , CM000675.2:g.48463741G= | GRCh38 |
| NC_000013.10:g.49037877G= , CM000675.1:g.49037877G= | GRCh37 |
| NC_000013.9:g.47935878G= | NCBI36 |
| NG_009009.1:g.164995G= , LRG_517:g.164995G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000321.3:c.2117G= MANE Select | NP_000312.2:p.Cys706= |
| ENST00000267163.6:c.2117G= MANE Select | ENSP00000267163.4:p.Cys706= |
| NM_000321.2:c.2117G= , LRG_517t1:c.2117G= | NP_000312.2:p.Cys706= |
| ENST00000267163.4:c.2117G= | ENSP00000267163.4:p.Cys706= |
| ENST00000643064.1:c.194+82298G= | |
| ENST00000650461.1:c.2117G= | ENSP00000497193.1:p.Cys706= |
| XM_011535171.1:c.1856G= | XP_011533473.1:p.Cys619= |
| XM_011535171.2:c.1856G= | XP_011533473.1:p.Cys619= |