Canonical Allele Identifier: CA185688671
Gene:

Linked Data

dbSNP Id: rs540620588

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.126999544C>T , CM000670.2:g.126999544C>T GRCh38
NC_000008.10:g.128011789C>T , CM000670.1:g.128011789C>T GRCh37
NC_000008.9:g.128080971C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746076.2:n.1301-7011C>T