Canonical Allele Identifier: CA2716564731
Gene:

Linked Data

dbSNP Id: rs2128863244

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.20129997T>A , CM000670.2:g.20129997T>A GRCh38
NC_000008.10:g.19987508T>A , CM000670.1:g.19987508T>A GRCh37
NC_000008.9:g.20031788T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949563.1:n.3408+78T>A
XR_949563.2:n.3400+78T>A