Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.55096480C>T , CM000666.2:g.55096480C>T | GRCh38 |
| NC_000004.11:g.55962647C>T , CM000666.1:g.55962647C>T | GRCh37 |
| NC_000004.10:g.55657404C>T | NCBI36 |
| NG_012004.1:g.34116G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263923.5:c.2615-138G>A MANE Select | ENSP00000263923.4:n.2615-138G>A | |
| ENST00000647068.1:n.2628-138G>A | ||
| ENST00000263923.4:c.2615-138G>A | ENSP00000263923.4:n.2615-138G>A | |
| ENST00000509309.1:n.241G>A | ||
| NM_002253.2:c.2615-138G>A | NP_002244.1:n.2615-138G>A | |
| NM_002253.3:c.2615-138G>A | NP_002244.1:n.2615-138G>A | |
| NM_002253.4:c.2615-138G>A MANE Select | NP_002244.1:n.2615-138G>A |