Canonical Allele Identifier: CA4980452

Gene: GLDC

Linked Data

• dbSNP Id: rs752141124
• ExAC: 9:6558635 T / C
• gnomAD v2: 9-6558635-T-C
• gnomAD v4: 9-6558635-T-C
• MyVariant Identifiers: chr9:g.6558635T>C (hg19) ; chr9:g.6558635T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6558635T>C , CM000671.2:g.6558635T>C	GRCh38
NC_000009.11:g.6558635T>C , CM000671.1:g.6558635T>C	GRCh37
NC_000009.10:g.6548635T>C	NCBI36
NG_016397.1:g.92058A>G , LRG_643:g.92058A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.1976A>G MANE Select	ENSP00000370737.4:p.His659Arg
ENST00000460457.2:n.136A>G
ENST00000638233.1:n.411A>G
ENST00000638661.1:c.176A>G	ENSP00000491369.1:p.His59Arg
ENST00000638694.1:n.163A>G
ENST00000639318.1:c.176A>G	ENSP00000491932.1:p.His59Arg
ENST00000639364.1:n.1676A>G
ENST00000639443.1:n.1544A>G
ENST00000639954.1:n.1684A>G
ENST00000640208.1:c.176A>G	ENSP00000491895.1:p.His59Arg
ENST00000640505.1:n.215A>G
ENST00000640592.1:n.1859A>G
ENST00000321612.6:c.1976A>G	ENSP00000370737.3:p.His659Arg
ENST00000460457.1:n.115A>G
NM_000170.2:c.1976A>G , LRG_643t1:c.1976A>G	NP_000161.2:p.His659Arg
NM_000170.3:c.1976A>G MANE Select	NP_000161.2:p.His659Arg