Canonical Allele Identifier: CA890857224
Gene:

Linked Data

dbSNP Id: rs1477774632

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168649352C>G , CM000663.2:g.168649352C>G GRCh38
NC_000001.10:g.168618590C>G , CM000663.1:g.168618590C>G GRCh37
NC_000001.9:g.166885214C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_922259.1:n.201-8077G>C
XR_922259.2:n.332-8077G>C