Canonical Allele Identifier: CA13449344
Gene:

Linked Data

dbSNP Id: rs11214105

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112166930G>A , CM000673.2:g.112166930G>A GRCh38
NC_000011.9:g.112037653G>A , CM000673.1:g.112037653G>A GRCh37
NC_000011.8:g.111542863G>A NCBI36
NG_028143.1:g.2188C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000525987.5:n.320-3489G>A
ENST00000531744.5:c.315-3489G>A ENSP00000456957.1:n.315-3489G>A
ENST00000532699.1:c.315-3489G>A ENSP00000456434.1:n.315-3489G>A