Canonical Allele Identifier: CA337715261
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs111696152

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12500272C>A , CM000686.2:g.12500272C>A GRCh38
NC_000024.9:g.14612066C>A , CM000686.1:g.14612066C>A GRCh37
NC_000024.8:g.13122074C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000381172.3:n.61+7037G>T