Canonical Allele Identifier: CA1609069938
Gene:

Linked Data

dbSNP Id: rs1765600554

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8525140G>A , CM000668.2:g.8525140G>A GRCh38
NC_000006.11:g.8525373G>A , CM000668.1:g.8525373G>A GRCh37
NC_000006.10:g.8470372G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038979.1:n.626-33445G>A
NR_038980.1:n.649-33445G>A