Canonical Allele Identifier: CA287548496
Gene:

Linked Data

dbSNP Id: rs954103167

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8137408T>C , CM000679.2:g.8137408T>C GRCh38
NC_000017.10:g.8040726T>C , CM000679.1:g.8040726T>C GRCh37
NC_000017.9:g.7981451T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934202.1:n.183-1441T>C
XR_934203.1:n.70-2069T>C
XR_934202.2:n.414-1441T>C