Canonical Allele Identifier: CA712744425
Gene: IVD HGNC NCBI

Linked Data

dbSNP Id: rs1218108136

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40405741dup , CM000677.2:g.40405741dup GRCh38
NC_000015.9:g.40697942dup , CM000677.1:g.40697942dup GRCh37
NC_000015.8:g.38485234dup NCBI36
NG_011986.1:g.5257dup
NG_011986.2:g.5257dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000650656.1:c.-78dup ENSP00000498731.1:n.-78dup
ENST00000651168.1:c.-78dup ENSP00000499074.1:n.-78dup
NM_001159508.1:c.-78dup NP_001152980.1:n.-78dup
NM_002225.3:c.-78dup NP_002216.2:n.-78dup
XR_429453.2:n.24dup