Canonical Allele Identifier: CA1818149558
Gene:

Linked Data

dbSNP Id: rs1814936862

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.126999563T>C , CM000670.2:g.126999563T>C GRCh38
NC_000008.10:g.128011808T>C , CM000670.1:g.128011808T>C GRCh37
NC_000008.9:g.128080990T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746076.2:n.1301-6992T>C