Canonical Allele Identifier: CA601754094
Gene:

Linked Data

dbSNP Id: rs1296616321

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112166805dup , CM000673.2:g.112166805dup GRCh38
NC_000011.9:g.112037528dup , CM000673.1:g.112037528dup GRCh37
NC_000011.8:g.111542738dup NCBI36
NG_028143.1:g.2314dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000525987.5:n.320-3614dup
ENST00000531744.5:c.315-3614dup ENSP00000456957.1:n.315-3614dup
ENST00000532699.1:c.315-3614dup ENSP00000456434.1:n.315-3614dup