Canonical Allele Identifier: CA150046511

Gene: IYD

Linked Data

• dbSNP Id: rs571183281
• gnomAD v3: 6-150399129-T-C
• gnomAD v4: 6-150399129-T-C
• MyVariant Identifiers: chr6:g.150720265T>C (hg19) ; chr6:g.150399129T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150399129T>C , CM000668.2:g.150399129T>C	GRCh38
NC_000006.11:g.150720265T>C , CM000668.1:g.150720265T>C	GRCh37
NC_000006.10:g.150761958T>C	NCBI36
NG_016007.1:g.35238T>C
NG_016007.2:g.35238T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.*892T>C MANE Select	ENSP00000343763.4:n.*892T>C
ENST00000229447.9:c.*992T>C	ENSP00000229447.5:n.*992T>C
ENST00000344419.7:c.*892T>C	ENSP00000343763.3:n.*892T>C
NM_001164694.1:c.*992T>C	NP_001158166.1:n.*992T>C
NM_001164695.1:c.*1079T>C	NP_001158167.1:n.*1079T>C
NM_203395.2:c.*892T>C	NP_981932.1:n.*892T>C
NM_001318495.1:c.*892T>C	NP_001305424.1:n.*892T>C
NR_134655.1:n.2075T>C
NM_001164694.2:c.*992T>C	NP_001158166.1:n.*992T>C
NM_001164695.2:c.*1079T>C	NP_001158167.1:n.*1079T>C
NM_001318495.2:c.*892T>C	NP_001305424.1:n.*892T>C
NM_203395.3:c.*892T>C MANE Select	NP_981932.1:n.*892T>C
NR_134655.2:n.1955T>C