Canonical Allele Identifier: CA372894197
Gene: GLDC HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.6595014C>G (hg19) chr9:g.6595014C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6595014C>G , CM000671.2:g.6595014C>G GRCh38
NC_000009.11:g.6595014C>G , CM000671.1:g.6595014C>G GRCh37
NC_000009.10:g.6585014C>G NCBI36
NG_016397.1:g.55679G>C , LRG_643:g.55679G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000321612.8:c.1261G>C MANE Select ENSP00000370737.4:p.Gly421Arg
ENST00000639364.1:n.961G>C
ENST00000639443.1:n.829G>C
ENST00000639493.1:n.413G>C
ENST00000639954.1:n.969G>C
ENST00000640592.1:n.1144G>C
ENST00000321612.6:c.1261G>C ENSP00000370737.3:p.Gly421Arg
ENST00000463305.1:n.345G>C
NM_000170.2:c.1261G>C , LRG_643t1:c.1261G>C NP_000161.2:p.Gly421Arg
NM_000170.3:c.1261G>C MANE Select NP_000161.2:p.Gly421Arg
Search 100 bp 5'
Search 100 bp 3'