Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.54495013C>A , CM000685.2:g.54495013C>A | GRCh38 |
| NC_000023.10:g.54521446C>A , CM000685.1:g.54521446C>A | GRCh37 |
| NC_000023.9:g.54538171C>A | NCBI36 |
| NG_008054.1:g.6154G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375135.4:c.307+113G>T MANE Select | ENSP00000364277.3:n.307+113G>T | |
| ENST00000375135.3:c.307+113G>T | ENSP00000364277.3:n.307+113G>T | |
| NM_004463.2:c.307+113G>T | NP_004454.2:n.307+113G>T | |
| NM_004463.3:c.307+113G>T MANE Select | NP_004454.2:n.307+113G>T |