Canonical Allele Identifier: CA10537433

Gene: IDS

Linked Data

• dbSNP Id: rs781803924
• ExAC: X:148564378 G / C
• gnomAD v2: X-148564378-G-C
• gnomAD v4: X-149482847-G-C
• MyVariant Identifiers: chrX:g.148564378G>C (hg19) ; chrX:g.149482847G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149482847G>C , CM000685.2:g.149482847G>C	GRCh38
NC_000023.10:g.148564378G>C , CM000685.1:g.148564378G>C	GRCh37
NC_000023.9:g.148372283G>C	NCBI36
NG_011900.3:g.27488C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1552C>G MANE Select	ENSP00000339801.6:p.His518Asp
ENST00000651111.1:c.919C>G	ENSP00000498395.1:p.His307Asp
ENST00000340855.10:c.1552C>G	ENSP00000339801.6:p.His518Asp
ENST00000422081.6:c.919C>G	ENSP00000477056.1:p.His307Asp
NM_000202.6:c.1552C>G	NP_000193.1:p.His518Asp
NM_001166550.2:c.1282C>G	NP_001160022.1:p.His428Asp
NM_000202.7:c.1552C>G	NP_000193.1:p.His518Asp
NM_001166550.3:c.1282C>G	NP_001160022.1:p.His428Asp
NM_000202.8:c.1552C>G MANE Select	NP_000193.1:p.His518Asp
NM_001166550.4:c.1282C>G	NP_001160022.1:p.His428Asp