Canonical Allele Identifier: CA1728106772
Gene:

Linked Data

dbSNP Id: rs1789258321

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.97388581G>T , CM000669.2:g.97388581G>T GRCh38
NC_000007.13:g.97017893G>T , CM000669.1:g.97017893G>T GRCh37
NC_000007.12:g.96855829G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745293.1:n.127-59934C>A