Canonical Allele Identifier: CA1775343163
Gene:

Linked Data

dbSNP Id: rs1802342804

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.33808376G>A , CM000670.2:g.33808376G>A GRCh38
NC_000008.10:g.33665894G>A , CM000670.1:g.33665894G>A GRCh37
NC_000008.9:g.33785436G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949659.1:n.240+11940G>A
XR_002956701.1:n.240+11940G>A