Canonical Allele Identifier: CA98367579
Gene:

Linked Data

dbSNP Id: rs571817456

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558325T>C , CM000666.2:g.62558325T>C GRCh38
NC_000004.11:g.63424043T>C , CM000666.1:g.63424043T>C GRCh37
NC_000004.10:g.63106638T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_938814.1:n.161-5519T>C