Canonical Allele Identifier: CA1033056781

Gene: GGCX

Linked Data

• dbSNP Id: rs1691754062
• gnomAD v3: 2-85547870-A-C
• gnomAD v4: 2-85547870-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85547870A>C , CM000664.2:g.85547870A>C	GRCh38
NC_000002.11:g.85774993A>C , CM000664.1:g.85774993A>C	GRCh37
NC_000002.10:g.85628504A>C	NCBI36
NG_011811.2:g.18665T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000233838.9:c.*2064T>G MANE Select	ENSP00000233838.3:n.*2064T>G
ENST00000233838.8:c.*2064T>G	ENSP00000233838.3:n.*2064T>G
ENST00000465637.5:n.313T>G
NM_000821.5:c.*2064T>G	NP_000812.2:n.*2064T>G
NM_000821.6:c.*2064T>G	NP_000812.2:n.*2064T>G
NM_001142269.2:c.*2064T>G	NP_001135741.1:n.*2064T>G
NM_001142269.3:c.*2064T>G	NP_001135741.1:n.*2064T>G
NM_000821.7:c.*2064T>G MANE Select	NP_000812.2:n.*2064T>G
NM_001142269.4:c.*2064T>G	NP_001135741.1:n.*2064T>G