Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.39207146T>C , CM000668.2:g.39207146T>C | GRCh38 |
| NC_000006.11:g.39174922T>C , CM000668.1:g.39174922T>C | GRCh37 |
| NC_000006.10:g.39282900T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_003740.4:c.187-11159A>G MANE Select | NP_003731.1:n.187-11159A>G |
| ENST00000359534.4:c.187-11159A>G MANE Select | ENSP00000352527.3:n.187-11159A>G |
| NM_003740.3:c.187-11159A>G | NP_003731.1:n.187-11159A>G |
| ENST00000359534.3:c.187-11159A>G | ENSP00000352527.3:n.187-11159A>G |
| XM_005249456.1:c.187-11159A>G | XP_005249513.1:n.187-11159A>G |