Canonical Allele Identifier: CA150046523

Gene: IYD

Linked Data

• dbSNP Id: rs371311730
• MyVariant Identifiers: chr6:g.150720291G>A (hg19) ; chr6:g.150399155G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150399155G>A , CM000668.2:g.150399155G>A	GRCh38
NC_000006.11:g.150720291G>A , CM000668.1:g.150720291G>A	GRCh37
NC_000006.10:g.150761984G>A	NCBI36
NG_016007.1:g.35264G>A
NG_016007.2:g.35264G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.*918G>A MANE Select	ENSP00000343763.4:n.*918G>A
ENST00000229447.9:c.*1018G>A	ENSP00000229447.5:n.*1018G>A
ENST00000344419.7:c.*918G>A	ENSP00000343763.3:n.*918G>A
NM_001164694.1:c.*1018G>A	NP_001158166.1:n.*1018G>A
NM_001164695.1:c.*1105G>A	NP_001158167.1:n.*1105G>A
NM_203395.2:c.*918G>A	NP_981932.1:n.*918G>A
NM_001318495.1:c.*918G>A	NP_001305424.1:n.*918G>A
NR_134655.1:n.2101G>A
NM_001164694.2:c.*1018G>A	NP_001158166.1:n.*1018G>A
NM_001164695.2:c.*1105G>A	NP_001158167.1:n.*1105G>A
NM_001318495.2:c.*918G>A	NP_001305424.1:n.*918G>A
NM_203395.3:c.*918G>A MANE Select	NP_981932.1:n.*918G>A
NR_134655.2:n.1981G>A