Canonical Allele Identifier: CA820731517

Gene: IYD

Linked Data

• dbSNP Id: rs1396969519
• gnomAD v3: 6-150398759-T-C
• gnomAD v4: 6-150398759-T-C
• MyVariant Identifiers: chr6:g.150719895T>C (hg19) ; chr6:g.150398759T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150398759T>C , CM000668.2:g.150398759T>C	GRCh38
NC_000006.11:g.150719895T>C , CM000668.1:g.150719895T>C	GRCh37
NC_000006.10:g.150761588T>C	NCBI36
NG_016007.1:g.34868T>C
NG_016007.2:g.34868T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.*522T>C MANE Select	ENSP00000343763.4:n.*522T>C
ENST00000229447.9:c.*622T>C	ENSP00000229447.5:n.*622T>C
ENST00000344419.7:c.*522T>C	ENSP00000343763.3:n.*522T>C
NM_001164694.1:c.*622T>C	NP_001158166.1:n.*622T>C
NM_001164695.1:c.*709T>C	NP_001158167.1:n.*709T>C
NM_203395.2:c.*522T>C	NP_981932.1:n.*522T>C
NM_001318495.1:c.*522T>C	NP_001305424.1:n.*522T>C
NR_134655.1:n.1705T>C
NM_001164694.2:c.*622T>C	NP_001158166.1:n.*622T>C
NM_001164695.2:c.*709T>C	NP_001158167.1:n.*709T>C
NM_001318495.2:c.*522T>C	NP_001305424.1:n.*522T>C
NM_203395.3:c.*522T>C MANE Select	NP_981932.1:n.*522T>C
NR_134655.2:n.1585T>C