Canonical Allele Identifier: CA1796404029
Gene:

Linked Data

dbSNP Id: rs1188404779

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.79191029C>A , CM000670.2:g.79191029C>A GRCh38
NC_000008.10:g.80103264C>A , CM000670.1:g.80103264C>A GRCh37
NC_000008.9:g.80265819C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745720.1:n.105+658C>A