Canonical Allele Identifier: CA1257242087
Gene:

Linked Data

dbSNP Id: rs1669085689

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.65440158G>A , CM000664.2:g.65440158G>A GRCh38
NC_000002.11:g.65667292G>A , CM000664.1:g.65667292G>A GRCh37
NC_000002.10:g.65520796G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940190.1:n.181+3276G>A
XR_940187.3:n.1439-73C>T