Canonical Allele Identifier: CA2293960142
Gene:

Linked Data

dbSNP Id: rs2031432843

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31756642G>A , CM000680.2:g.31756642G>A GRCh38
NC_000018.9:g.29336605G>A , CM000680.1:g.29336605G>A GRCh37
NC_000018.8:g.27590603G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935338.1:n.66-5497G>A