Canonical Allele Identifier: CA968965877
Gene: IVD HGNC NCBI

Linked Data

dbSNP Id: rs1890323328

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40405745C>T , CM000677.2:g.40405745C>T GRCh38
NC_000015.9:g.40697946C>T , CM000677.1:g.40697946C>T GRCh37
NC_000015.8:g.38485238C>T NCBI36
NG_011986.1:g.5261C>T
NG_011986.2:g.5261C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000650656.1:c.-74C>T ENSP00000498731.1:n.-74C>T
ENST00000651168.1:c.-74C>T ENSP00000499074.1:n.-74C>T
NM_001159508.1:c.-74C>T NP_001152980.1:n.-74C>T
NM_002225.3:c.-74C>T NP_002216.2:n.-74C>T
XR_429453.2:n.28C>T