Canonical Allele Identifier: CA856539055
Gene:

Linked Data

dbSNP Id: rs1212834144

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.88535710G>C , CM000670.2:g.88535710G>C GRCh38
NC_000008.10:g.89547939G>C , CM000670.1:g.89547939G>C GRCh37
NC_000008.9:g.89617055G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001745651.2:n.1673+10807C>G
XR_001745653.2:n.286-6970G>C
XR_928383.3:n.1475+10807C>G