Canonical Allele Identifier: CA1462694301
Gene:

Linked Data

dbSNP Id: rs753645472

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558272T>C , CM000666.2:g.62558272T>C GRCh38
NC_000004.11:g.63423990T>C , CM000666.1:g.63423990T>C GRCh37
NC_000004.10:g.63106585T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_938814.1:n.161-5572T>C