dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.160606796C>A , CM000668.2:g.160606796C>A | GRCh38 |
| NC_000006.11:g.161027828C>A , CM000668.1:g.161027828C>A | GRCh37 |
| NC_000006.10:g.160947818C>A | NCBI36 |
| NG_016147.1:g.64580G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000316300.10:c.2604-138G>T MANE Select | ENSP00000321334.6:n.2604-138G>T | |
| ENST00000316300.9:c.2604-138G>T | ENSP00000321334.5:n.2604-138G>T | |
| ENST00000447678.2:c.345-138G>T | ENSP00000395608.2:n.345-138G>T | |
| NM_005577.2:c.2604-138G>T | NP_005568.2:n.2604-138G>T | |
| NM_005577.3:c.2604-138G>T | NP_005568.2:n.2604-138G>T | |
| NM_005577.4:c.2604-138G>T MANE Select | NP_005568.2:n.2604-138G>T |