Canonical Allele Identifier: CA1728106684
Gene:

Linked Data

dbSNP Id: rs1789256421

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.97388378C>G , CM000669.2:g.97388378C>G GRCh38
NC_000007.13:g.97017690C>G , CM000669.1:g.97017690C>G GRCh37
NC_000007.12:g.96855626C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001745293.1:n.127-59731G>C