Canonical Allele Identifier: CA1728106767
Gene:

Linked Data

dbSNP Id: rs1789258215

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.97388564T>C , CM000669.2:g.97388564T>C GRCh38
NC_000007.13:g.97017876T>C , CM000669.1:g.97017876T>C GRCh37
NC_000007.12:g.96855812T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745293.1:n.127-59917A>G