Canonical Allele Identifier: CA2659852523

Gene: GGCX

Linked Data

• gnomAD v4: 2-85546513-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85546513T>C , CM000664.2:g.85546513T>C	GRCh38
NC_000002.11:g.85773636T>C , CM000664.1:g.85773636T>C	GRCh37
NC_000002.10:g.85627147T>C	NCBI36
NG_011811.2:g.20022A>G
NG_029183.1:g.12536T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233838.9:c.*3421A>G MANE Select	ENSP00000233838.3:n.*3421A>G
ENST00000233838.8:c.*3421A>G	ENSP00000233838.3:n.*3421A>G
NM_000821.5:c.*3421A>G	NP_000812.2:n.*3421A>G
NM_000821.6:c.*3421A>G	NP_000812.2:n.*3421A>G
NM_001142269.2:c.*3421A>G	NP_001135741.1:n.*3421A>G
NM_001142269.3:c.*3421A>G	NP_001135741.1:n.*3421A>G
NM_000821.7:c.*3421A>G MANE Select	NP_000812.2:n.*3421A>G
NM_001142269.4:c.*3421A>G	NP_001135741.1:n.*3421A>G