Canonical Allele Identifier: CA847111732
Gene:

Linked Data

dbSNP Id: rs1335789476

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.126999716G>T , CM000670.2:g.126999716G>T GRCh38
NC_000008.10:g.128011961G>T , CM000670.1:g.128011961G>T GRCh37
NC_000008.9:g.128081143G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746076.2:n.1301-6839G>T