Canonical Allele Identifier: CA98367585
Gene:

Linked Data

dbSNP Id: rs953793095

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558381T>C , CM000666.2:g.62558381T>C GRCh38
NC_000004.11:g.63424099T>C , CM000666.1:g.63424099T>C GRCh37
NC_000004.10:g.63106694T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_938814.1:n.161-5463T>C