Canonical Allele Identifier: CA2713856975
Gene:

Linked Data

dbSNP Id: rs1265218959

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.13400560T>C , CM000669.2:g.13400560T>C GRCh38
NC_000007.13:g.13440185T>C , CM000669.1:g.13440185T>C GRCh37
NC_000007.12:g.13406710T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001745097.1:n.147+90237T>C