Canonical Allele Identifier: CA1830493713
Gene: GLDC HGNC NCBI

Linked Data

dbSNP Id: rs372470287

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6556318G>C , CM000671.2:g.6556318G>C GRCh38
NC_000009.11:g.6556318G>C , CM000671.1:g.6556318G>C GRCh37
NC_000009.10:g.6546318G>C NCBI36
NG_016397.1:g.94375C>G , LRG_643:g.94375C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000321612.8:c.2053-16C>G MANE Select ENSP00000370737.4:n.2053-16C>G
ENST00000638233.1:n.488-16C>G
ENST00000638661.1:c.253-16C>G ENSP00000491369.1:n.253-16C>G
ENST00000638694.1:n.240-16C>G
ENST00000639318.1:c.253-16C>G ENSP00000491932.1:n.253-16C>G
ENST00000639364.1:n.1753-16C>G
ENST00000639443.1:n.1621-16C>G
ENST00000639954.1:n.1761-16C>G
ENST00000640505.1:n.292-16C>G
ENST00000321612.6:c.2053-16C>G ENSP00000370737.3:n.2053-16C>G
NM_000170.2:c.2053-16C>G , LRG_643t1:c.2053-16C>G NP_000161.2:n.2053-16C>G
NM_000170.3:c.2053-16C>G MANE Select NP_000161.2:n.2053-16C>G