Canonical Allele Identifier: CA2733843309
Gene:

Linked Data

dbSNP Id: rs2144613970

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50211615T>A , CM000679.2:g.50211615T>A GRCh38
NC_000017.10:g.48288976T>A , CM000679.1:g.48288976T>A GRCh37
NC_000017.9:g.45643975T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934838.1:n.42+2209T>A