Canonical Allele Identifier: CA1728106666
Gene:

Linked Data

dbSNP Id: rs1789255971

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.97388333T>C , CM000669.2:g.97388333T>C GRCh38
NC_000007.13:g.97017645T>C , CM000669.1:g.97017645T>C GRCh37
NC_000007.12:g.96855581T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001745293.1:n.127-59686A>G