Canonical Allele Identifier: CA1728106722
Gene:

Linked Data

dbSNP Id: rs776665099

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.97388450T>G , CM000669.2:g.97388450T>G GRCh38
NC_000007.13:g.97017762T>G , CM000669.1:g.97017762T>G GRCh37
NC_000007.12:g.96855698T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001745293.1:n.127-59803A>C