Canonical Allele Identifier: CA2733843380
Gene:

Linked Data

dbSNP Id: rs2144613978

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50211627T>A , CM000679.2:g.50211627T>A GRCh38
NC_000017.10:g.48288988T>A , CM000679.1:g.48288988T>A GRCh37
NC_000017.9:g.45643987T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_934838.1:n.43-2208T>A