Canonical Allele Identifier: CA1595158905
Gene:

Linked Data

dbSNP Id: rs1757448859

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159580589dup , CM000667.2:g.159580589dup GRCh38
NC_000005.9:g.159007597dup , CM000667.1:g.159007597dup GRCh37
NC_000005.8:g.158940175dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_941139.1:n.2075+154dup
XR_941140.1:n.2075+154dup
XR_941141.1:n.570+154dup
XR_941139.2:n.2229+154dup