Canonical Allele Identifier: CA1672406170

Gene: IYD

Linked Data

• dbSNP Id: rs558132966
• gnomAD v4: 6-150398972-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150398972T>C , CM000668.2:g.150398972T>C	GRCh38
NC_000006.11:g.150720108T>C , CM000668.1:g.150720108T>C	GRCh37
NC_000006.10:g.150761801T>C	NCBI36
NG_016007.1:g.35081T>C
NG_016007.2:g.35081T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.*735T>C MANE Select	ENSP00000343763.4:n.*735T>C
ENST00000229447.9:c.*835T>C	ENSP00000229447.5:n.*835T>C
ENST00000344419.7:c.*735T>C	ENSP00000343763.3:n.*735T>C
NM_001164694.1:c.*835T>C	NP_001158166.1:n.*835T>C
NM_001164695.1:c.*922T>C	NP_001158167.1:n.*922T>C
NM_203395.2:c.*735T>C	NP_981932.1:n.*735T>C
NM_001318495.1:c.*735T>C	NP_001305424.1:n.*735T>C
NR_134655.1:n.1918T>C
NM_001164694.2:c.*835T>C	NP_001158166.1:n.*835T>C
NM_001164695.2:c.*922T>C	NP_001158167.1:n.*922T>C
NM_001318495.2:c.*735T>C	NP_001305424.1:n.*735T>C
NM_203395.3:c.*735T>C MANE Select	NP_981932.1:n.*735T>C
NR_134655.2:n.1798T>C