Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.12887176T>C , CM000681.2:g.12887176T>C | GRCh38 |
| NC_000019.9:g.12997990T>C , CM000681.1:g.12997990T>C | GRCh37 |
| NC_000019.8:g.12858990T>C | NCBI36 |
| NG_009292.1:g.1017T>C | |
| NG_013087.1:g.5028A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264834.6:c.-36A>G MANE Select | ENSP00000264834.3:n.-36A>G | |
| ENST00000264834.4:c.-36A>G | ENSP00000264834.3:n.-36A>G | |
| NM_006563.3:c.-36A>G | NP_006554.1:n.-36A>G | |
| NM_006563.4:c.-36A>G | NP_006554.1:n.-36A>G | |
| NM_006563.5:c.-36A>G MANE Select | NP_006554.1:n.-36A>G |