Canonical Allele Identifier: CA712744444
Gene: IVD HGNC NCBI

Linked Data

dbSNP Id: rs543369127

Genomic Alleles

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

Transcript Alleles

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