Canonical Allele Identifier: CA1672405998
Gene: IYD HGNC NCBI

Linked Data

dbSNP Id: rs1582807019

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.150398602G>A , CM000668.2:g.150398602G>A GRCh38
NC_000006.11:g.150719738G>A , CM000668.1:g.150719738G>A GRCh37
NC_000006.10:g.150761431G>A NCBI36
NG_016007.1:g.34711G>A
NG_016007.2:g.34711G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000344419.8:c.*365G>A MANE Select ENSP00000343763.4:n.*365G>A
ENST00000229447.9:c.*465G>A ENSP00000229447.5:n.*465G>A
ENST00000344419.7:c.*365G>A ENSP00000343763.3:n.*365G>A
NM_001164694.1:c.*465G>A NP_001158166.1:n.*465G>A
NM_001164695.1:c.*552G>A NP_001158167.1:n.*552G>A
NM_203395.2:c.*365G>A NP_981932.1:n.*365G>A
NM_001318495.1:c.*365G>A NP_001305424.1:n.*365G>A
NR_134655.1:n.1548G>A
NM_001164694.2:c.*465G>A NP_001158166.1:n.*465G>A
NM_001164695.2:c.*552G>A NP_001158167.1:n.*552G>A
NM_001318495.2:c.*365G>A NP_001305424.1:n.*365G>A
NM_203395.3:c.*365G>A MANE Select NP_981932.1:n.*365G>A
NR_134655.2:n.1428G>A