Canonical Allele Identifier: CA185688668
Gene:

Linked Data

dbSNP Id: rs904860465

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.126999526C>T , CM000670.2:g.126999526C>T GRCh38
NC_000008.10:g.128011771C>T , CM000670.1:g.128011771C>T GRCh37
NC_000008.9:g.128080953C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746076.2:n.1301-7029C>T