Canonical Allele Identifier: CA1672978992
Gene:

Linked Data

dbSNP Id: rs1777185146

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151633434G>A , CM000668.2:g.151633434G>A GRCh38
NC_000006.11:g.151954569G>A , CM000668.1:g.151954569G>A GRCh37
NC_000006.10:g.151996262G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943115.1:n.2496+3452G>A