Canonical Allele Identifier: CA1691656433
Gene:

Linked Data

dbSNP Id: rs1803285459

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17957832T>C , CM000669.2:g.17957832T>C GRCh38
NC_000007.13:g.17997455T>C , CM000669.1:g.17997455T>C GRCh37
NC_000007.12:g.17963980T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_927078.1:n.271-838T>C