Canonical Allele Identifier: CA820731579

Gene: IYD

Linked Data

• dbSNP Id: rs1389544955
• gnomAD v3: 6-150398871-A-T
• gnomAD v4: 6-150398871-A-T
• MyVariant Identifiers: chr6:g.150720007A>T (hg19) ; chr6:g.150398871A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150398871A>T , CM000668.2:g.150398871A>T	GRCh38
NC_000006.11:g.150720007A>T , CM000668.1:g.150720007A>T	GRCh37
NC_000006.10:g.150761700A>T	NCBI36
NG_016007.1:g.34980A>T
NG_016007.2:g.34980A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.*634A>T MANE Select	ENSP00000343763.4:n.*634A>T
ENST00000229447.9:c.*734A>T	ENSP00000229447.5:n.*734A>T
ENST00000344419.7:c.*634A>T	ENSP00000343763.3:n.*634A>T
NM_001164694.1:c.*734A>T	NP_001158166.1:n.*734A>T
NM_001164695.1:c.*821A>T	NP_001158167.1:n.*821A>T
NM_203395.2:c.*634A>T	NP_981932.1:n.*634A>T
NM_001318495.1:c.*634A>T	NP_001305424.1:n.*634A>T
NR_134655.1:n.1817A>T
NM_001164694.2:c.*734A>T	NP_001158166.1:n.*734A>T
NM_001164695.2:c.*821A>T	NP_001158167.1:n.*821A>T
NM_001318495.2:c.*634A>T	NP_001305424.1:n.*634A>T
NM_203395.3:c.*634A>T MANE Select	NP_981932.1:n.*634A>T
NR_134655.2:n.1697A>T