Canonical Allele Identifier: CA721980878
Gene:

Linked Data

dbSNP Id: rs1409774619

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56610686G>A , CM000678.2:g.56610686G>A GRCh38
NC_000016.9:g.56644598G>A , CM000678.1:g.56644598G>A GRCh37
NC_000016.8:g.55202099G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_933616.1:n.605+630C>T