Canonical Allele Identifier: CA2246165950
Gene:

Linked Data

dbSNP Id: rs1254598006

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8137718C>A , CM000679.2:g.8137718C>A GRCh38
NC_000017.10:g.8041036C>A , CM000679.1:g.8041036C>A GRCh37
NC_000017.9:g.7981761C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_934202.1:n.183-1131C>A
XR_934203.1:n.70-1759C>A
XR_934202.2:n.414-1131C>A