Canonical Allele Identifier: CA2171763180
Gene: IVD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40405760G= , CM000677.2:g.40405760G= GRCh38
NC_000015.9:g.40697961G= , CM000677.1:g.40697961G= GRCh37
NC_000015.8:g.38485253G= NCBI36
NG_011986.1:g.5276G=
NG_011986.2:g.5276G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650656.1:c.-59G= ENSP00000498731.1:n.-59G=
ENST00000651168.1:c.-59G= ENSP00000499074.1:n.-59G=
NM_001159508.1:c.-59G= NP_001152980.1:n.-59G=
NM_002225.3:c.-59G= NP_002216.2:n.-59G=
XR_429453.2:n.43G=