Canonical Allele Identifier: CA150046132

Gene: IYD

Linked Data

• dbSNP Id: rs1044855221
• MyVariant Identifiers: chr6:g.150719913C>G (hg19) ; chr6:g.150398777C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150398777C>G , CM000668.2:g.150398777C>G	GRCh38
NC_000006.11:g.150719913C>G , CM000668.1:g.150719913C>G	GRCh37
NC_000006.10:g.150761606C>G	NCBI36
NG_016007.1:g.34886C>G
NG_016007.2:g.34886C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.*540C>G MANE Select	ENSP00000343763.4:n.*540C>G
ENST00000229447.9:c.*640C>G	ENSP00000229447.5:n.*640C>G
ENST00000344419.7:c.*540C>G	ENSP00000343763.3:n.*540C>G
NM_001164694.1:c.*640C>G	NP_001158166.1:n.*640C>G
NM_001164695.1:c.*727C>G	NP_001158167.1:n.*727C>G
NM_203395.2:c.*540C>G	NP_981932.1:n.*540C>G
NM_001318495.1:c.*540C>G	NP_001305424.1:n.*540C>G
NR_134655.1:n.1723C>G
NM_001164694.2:c.*640C>G	NP_001158166.1:n.*640C>G
NM_001164695.2:c.*727C>G	NP_001158167.1:n.*727C>G
NM_001318495.2:c.*540C>G	NP_001305424.1:n.*540C>G
NM_203395.3:c.*540C>G MANE Select	NP_981932.1:n.*540C>G
NR_134655.2:n.1603C>G