Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57133430T>C , CM000674.2:g.57133430T>C | GRCh38 |
| NC_000012.11:g.57527213T>C , CM000674.1:g.57527213T>C | GRCh37 |
| NC_000012.10:g.55813480T>C | NCBI36 |
| NG_016444.1:g.9932T>C | |
| NG_021272.2:g.3710A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000243077.8:c.67+4399T>C MANE Select | ENSP00000243077.3:n.67+4399T>C | |
| ENST00000243077.7:c.67+4399T>C | ENSP00000243077.3:n.67+4399T>C | |
| ENST00000338962.8:c.67+4399T>C | ENSP00000341264.4:n.67+4399T>C | |
| ENST00000553277.5:c.67+4399T>C | ENSP00000451449.1:n.67+4399T>C | |
| ENST00000554174.1:c.67+4399T>C | ENSP00000451737.1:n.67+4399T>C | |
| NM_002332.2:c.67+4399T>C | NP_002323.2:n.67+4399T>C | |
| XM_017019303.1:c.67+4399T>C | XP_016874792.1:n.67+4399T>C | |
| NM_002332.3:c.67+4399T>C MANE Select | NP_002323.2:n.67+4399T>C |