Canonical Allele Identifier: CA2171763177
Gene: IVD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40405754T= , CM000677.2:g.40405754T= GRCh38
NC_000015.9:g.40697955T= , CM000677.1:g.40697955T= GRCh37
NC_000015.8:g.38485247T= NCBI36
NG_011986.1:g.5270T=
NG_011986.2:g.5270T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650656.1:c.-65T= ENSP00000498731.1:n.-65T=
ENST00000651168.1:c.-65T= ENSP00000499074.1:n.-65T=
NM_001159508.1:c.-65T= NP_001152980.1:n.-65T=
NM_002225.3:c.-65T= NP_002216.2:n.-65T=
XR_429453.2:n.37T=