Canonical Allele Identifier: CA185688696
Gene:

Linked Data

dbSNP Id: rs560657125

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.126999683G>C , CM000670.2:g.126999683G>C GRCh38
NC_000008.10:g.128011928G>C , CM000670.1:g.128011928G>C GRCh37
NC_000008.9:g.128081110G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746076.2:n.1301-6872G>C