Canonical Allele Identifier: CA773963146
Gene:

Linked Data

dbSNP Id: rs1286576928

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63506430G>A , CM000679.2:g.63506430G>A GRCh38
NC_000017.10:g.61583791G>A , CM000679.1:g.61583791G>A GRCh37
NC_000017.9:g.58937523G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577647.2:c.1970-626G>A ENSP00000464149.1:n.1970-626G>A