Canonical Allele Identifier: CA2343599299
Gene:

Linked Data

dbSNP Id: rs1989135862

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55754323G>A , CM000681.2:g.55754323G>A GRCh38
NC_000019.9:g.56265689G>A , CM000681.1:g.56265689G>A GRCh37
NC_000019.8:g.60957501G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_936081.1:n.192G>A
XR_936081.2:n.251G>A