Canonical Allele Identifier: CA1728106731
Gene:

Linked Data

dbSNP Id: rs1789257404

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.97388481C>G , CM000669.2:g.97388481C>G GRCh38
NC_000007.13:g.97017793C>G , CM000669.1:g.97017793C>G GRCh37
NC_000007.12:g.96855729C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745293.1:n.127-59834G>C