Canonical Allele Identifier: CA820731508

Gene: IYD

Linked Data

• dbSNP Id: rs1384388072
• MyVariant Identifiers: chr6:g.150719859A>G (hg19) ; chr6:g.150398723A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150398723A>G , CM000668.2:g.150398723A>G	GRCh38
NC_000006.11:g.150719859A>G , CM000668.1:g.150719859A>G	GRCh37
NC_000006.10:g.150761552A>G	NCBI36
NG_016007.1:g.34832A>G
NG_016007.2:g.34832A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.*486A>G MANE Select	ENSP00000343763.4:n.*486A>G
ENST00000229447.9:c.*586A>G	ENSP00000229447.5:n.*586A>G
ENST00000344419.7:c.*486A>G	ENSP00000343763.3:n.*486A>G
NM_001164694.1:c.*586A>G	NP_001158166.1:n.*586A>G
NM_001164695.1:c.*673A>G	NP_001158167.1:n.*673A>G
NM_203395.2:c.*486A>G	NP_981932.1:n.*486A>G
NM_001318495.1:c.*486A>G	NP_001305424.1:n.*486A>G
NR_134655.1:n.1669A>G
NM_001164694.2:c.*586A>G	NP_001158166.1:n.*586A>G
NM_001164695.2:c.*673A>G	NP_001158167.1:n.*673A>G
NM_001318495.2:c.*486A>G	NP_001305424.1:n.*486A>G
NM_203395.3:c.*486A>G MANE Select	NP_981932.1:n.*486A>G
NR_134655.2:n.1549A>G