Canonical Allele Identifier: CA865903114
Gene: GLDC HGNC NCBI

Linked Data

dbSNP Id: rs1434732529
gnomAD v4: 9-6556380-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6556380T>C , CM000671.2:g.6556380T>C GRCh38
NC_000009.11:g.6556380T>C , CM000671.1:g.6556380T>C GRCh37
NC_000009.10:g.6546380T>C NCBI36
NG_016397.1:g.94313A>G , LRG_643:g.94313A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000321612.8:c.2053-78A>G MANE Select ENSP00000370737.4:n.2053-78A>G
ENST00000638233.1:n.488-78A>G
ENST00000638661.1:c.253-78A>G ENSP00000491369.1:n.253-78A>G
ENST00000638694.1:n.240-78A>G
ENST00000639318.1:c.253-78A>G ENSP00000491932.1:n.253-78A>G
ENST00000639364.1:n.1753-78A>G
ENST00000639443.1:n.1621-78A>G
ENST00000639954.1:n.1761-78A>G
ENST00000640505.1:n.292-78A>G
ENST00000321612.6:c.2053-78A>G ENSP00000370737.3:n.2053-78A>G
NM_000170.2:c.2053-78A>G , LRG_643t1:c.2053-78A>G NP_000161.2:n.2053-78A>G
NM_000170.3:c.2053-78A>G MANE Select NP_000161.2:n.2053-78A>G