Canonical Allele Identifier: CA98367598
Gene:

Linked Data

dbSNP Id: rs868508005

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558458A>C , CM000666.2:g.62558458A>C GRCh38
NC_000004.11:g.63424176A>C , CM000666.1:g.63424176A>C GRCh37
NC_000004.10:g.63106771A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5386A>C