Canonical Allele Identifier: CA452567361
Gene: IYD HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.150710579T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.150389443T>G , CM000668.2:g.150389443T>G GRCh38
NC_000006.11:g.150710579T>G , CM000668.1:g.150710579T>G GRCh37
NC_000006.10:g.150752272T>G NCBI36
NG_016007.1:g.25552T>G
NG_016007.2:g.25552T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000344419.8:c.270T>G MANE Select ENSP00000343763.4:p.Ser90=
ENST00000229447.9:c.270T>G ENSP00000229447.5:p.Ser90=
ENST00000344419.7:c.270T>G ENSP00000343763.3:p.Ser90=
ENST00000367335.7:c.270T>G ENSP00000356304.3:p.Ser90=
ENST00000392255.7:c.270T>G ENSP00000376084.3:p.Ser90=
ENST00000392256.6:c.270T>G ENSP00000376085.2:p.Ser90=
ENST00000422583.2:c.147T>G ENSP00000397342.2:p.Ser49=
ENST00000425615.3:c.105T>G ENSP00000390081.3:p.Ser35=
ENST00000500320.7:c.270T>G ENSP00000441276.1:p.Ser90=
ENST00000546121.1:n.213T>G
NM_001164694.1:c.270T>G NP_001158166.1:p.Ser90=
NM_001164695.1:c.270T>G NP_001158167.1:p.Ser90=
NM_203395.2:c.270T>G NP_981932.1:p.Ser90=
XM_006715478.2:c.270T>G XP_006715541.1:p.Ser90=
XM_006715479.2:c.105T>G XP_006715542.1:p.Ser35=
XR_245516.3:n.433T>G
NM_001318495.1:c.92T>G NP_001305424.1:p.Leu31Arg
NR_134655.1:n.410T>G
XM_006715478.3:c.270T>G XP_006715541.1:p.Ser90=
XM_006715479.3:c.105T>G XP_006715542.1:p.Ser35=
NM_001164694.2:c.270T>G NP_001158166.1:p.Ser90=
NM_001164695.2:c.270T>G NP_001158167.1:p.Ser90=
NM_001318495.2:c.92T>G NP_001305424.1:p.Leu31Arg
NM_203395.3:c.270T>G MANE Select NP_981932.1:p.Ser90=
NR_134655.2:n.290T>G