Canonical Allele Identifier: CA2171763170
Gene: IVD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40405746C= , CM000677.2:g.40405746C= GRCh38
NC_000015.9:g.40697947C= , CM000677.1:g.40697947C= GRCh37
NC_000015.8:g.38485239C= NCBI36
NG_011986.1:g.5262C=
NG_011986.2:g.5262C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650656.1:c.-73C= ENSP00000498731.1:n.-73C=
ENST00000651168.1:c.-73C= ENSP00000499074.1:n.-73C=
NM_001159508.1:c.-73C= NP_001152980.1:n.-73C=
NM_002225.3:c.-73C= NP_002216.2:n.-73C=
XR_429453.2:n.29C=