Canonical Allele Identifier: CA984456438
Gene:

Linked Data

dbSNP Id: rs1770167906

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50211867C>A , CM000679.2:g.50211867C>A GRCh38
NC_000017.10:g.48289228C>A , CM000679.1:g.48289228C>A GRCh37
NC_000017.9:g.45644227C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934838.1:n.43-1968C>A