Canonical Allele Identifier: CA12583759
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs11763963

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.26605814T>C , CM000669.2:g.26605814T>C GRCh38
NC_000007.13:g.26645433T>C , CM000669.1:g.26645433T>C GRCh37
NC_000007.12:g.26611958T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_927131.1:n.1118-6444A>G
XR_927131.2:n.1186-6444A>G