Canonical Allele Identifier: CA849634461
Gene:

Linked Data

dbSNP Id: rs1402532680

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.20130136A>G , CM000670.2:g.20130136A>G GRCh38
NC_000008.10:g.19987647A>G , CM000670.1:g.19987647A>G GRCh37
NC_000008.9:g.20031927A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949563.1:n.3408+217A>G
XR_949563.2:n.3400+217A>G