Canonical Allele Identifier: CA150046365

Gene: IYD

Linked Data

• dbSNP Id: rs529474029
• MyVariant Identifiers: chr6:g.150720165C>A (hg19) ; chr6:g.150399029C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150399029C>A , CM000668.2:g.150399029C>A	GRCh38
NC_000006.11:g.150720165C>A , CM000668.1:g.150720165C>A	GRCh37
NC_000006.10:g.150761858C>A	NCBI36
NG_016007.1:g.35138C>A
NG_016007.2:g.35138C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.*792C>A MANE Select	ENSP00000343763.4:n.*792C>A
ENST00000229447.9:c.*892C>A	ENSP00000229447.5:n.*892C>A
ENST00000344419.7:c.*792C>A	ENSP00000343763.3:n.*792C>A
NM_001164694.1:c.*892C>A	NP_001158166.1:n.*892C>A
NM_001164695.1:c.*979C>A	NP_001158167.1:n.*979C>A
NM_203395.2:c.*792C>A	NP_981932.1:n.*792C>A
NM_001318495.1:c.*792C>A	NP_001305424.1:n.*792C>A
NR_134655.1:n.1975C>A
NM_001164694.2:c.*892C>A	NP_001158166.1:n.*892C>A
NM_001164695.2:c.*979C>A	NP_001158167.1:n.*979C>A
NM_001318495.2:c.*792C>A	NP_001305424.1:n.*792C>A
NM_203395.3:c.*792C>A MANE Select	NP_981932.1:n.*792C>A
NR_134655.2:n.1855C>A