Canonical Allele Identifier: CA1769199462
Gene:

Linked Data

dbSNP Id: rs2071239862

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.20130139C>G , CM000670.2:g.20130139C>G GRCh38
NC_000008.10:g.19987650C>G , CM000670.1:g.19987650C>G GRCh37
NC_000008.9:g.20031930C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949563.1:n.3408+220C>G
XR_949563.2:n.3400+220C>G