Canonical Allele Identifier: CA1715429645
Gene:

Linked Data

dbSNP Id: rs1788208332

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.69146926T>G , CM000669.2:g.69146926T>G GRCh38
NC_000007.13:g.68611913T>G , CM000669.1:g.68611913T>G GRCh37
NC_000007.12:g.68249849T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_927647.1:n.88-800A>C