Canonical Allele Identifier: CA1929213294
Gene:

Linked Data

dbSNP Id: rs1848181955

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762469G>A , CM000672.2:g.94762469G>A GRCh38
NC_000010.10:g.96522226G>A , CM000672.1:g.96522226G>A GRCh37
NC_000010.9:g.96512216G>A NCBI36
NG_008384.2:g.4764G>A
NG_008384.3:g.4789G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000464755.1:c.932-12589G>A ENSP00000483243.1:n.932-12589G>A