Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.30845125T>C , CM000665.2:g.30845125T>C | GRCh38 |
| NC_000003.11:g.30886617T>C , CM000665.1:g.30886617T>C | GRCh37 |
| NC_000003.10:g.30861621T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000282538.10:c.652-659A>G MANE Select | ENSP00000282538.5:n.652-659A>G | |
| ENST00000282538.9:c.652-659A>G | ENSP00000282538.5:n.652-659A>G | |
| ENST00000454381.3:c.652-659A>G | ENSP00000427059.1:n.652-659A>G | |
| NM_207359.2:c.652-659A>G | NP_997242.2:n.652-659A>G | |
| XM_017006297.1:c.595-659A>G | XP_016861786.1:n.595-659A>G | |
| XM_017006298.1:c.-7-861A>G | XP_016861787.1:n.-7-861A>G | |
| NM_207359.3:c.652-659A>G MANE Select | NP_997242.2:n.652-659A>G |