Canonical Allele Identifier: CA1615804342
Gene:

Linked Data

dbSNP Id: rs1762376671

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.23077102T>C , CM000668.2:g.23077102T>C GRCh38
NC_000006.11:g.23077330T>C , CM000668.1:g.23077330T>C GRCh37
NC_000006.10:g.23185309T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926583.1:n.246-20035A>G
XR_926584.1:n.246-60282A>G
XR_926583.2:n.246-20035A>G