Canonical Allele Identifier:
CA2838201235
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.161610494C>T , CM000663.2:g.161610494C>T | GRCh38 |
| NC_000001.10:g.161580284C>T , CM000663.1:g.161580284C>T | GRCh37 |
| NC_000001.9:g.159846908C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000699402.1:c.40+20561G>A | ENSP00000514363.1:n.40+20561G>A | |
| ENST00000699403.1:c.61+19874G>A | ENSP00000514364.1:n.61+19874G>A |