Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.98585736T>G , CM000665.2:g.98585736T>G | GRCh38 |
| NC_000003.11:g.98304580T>G , CM000665.1:g.98304580T>G | GRCh37 |
| NC_000003.10:g.99787270T>G | NCBI36 |
| NG_015994.1:g.12876A>C | |
| NG_015994.2:g.12876A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647941.2:c.954-77A>C MANE Select | ENSP00000497326.1:n.954-77A>C | |
| ENST00000264193.2:c.954-77A>C | ENSP00000264193.2:n.954-77A>C | |
| ENST00000510489.1:n.127A>C | ||
| NM_000097.5:c.954-77A>C | NP_000088.3:n.954-77A>C | |
| XM_005247125.3:c.954-77A>C | XP_005247182.1:n.954-77A>C | |
| NM_000097.7:c.954-77A>C MANE Select | NP_000088.3:n.954-77A>C | |
| XM_005247125.4:c.954-77A>C | XP_005247182.1:n.954-77A>C | |
| XR_001740025.2:n.1125-77A>C | ||
| XR_001740026.1:n.1612A>C | ||
| XR_001740027.1:n.1229-77A>C | ||
| XR_001740028.1:n.1195-77A>C |