Canonical Allele Identifier: CA1619157164
Gene:

Linked Data

dbSNP Id: rs1761791253

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31440043A>C , CM000668.2:g.31440043A>C GRCh38
NC_000006.11:g.31407820A>C , CM000668.1:g.31407820A>C GRCh37
NC_000006.10:g.31515799A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926694.1:n.64T>G