Canonical Allele Identifier: CA51728829

Gene: GGCX

Linked Data

• dbSNP Id: rs897439627
• gnomAD v2: 2-85773073-T-G
• gnomAD v3: 2-85545950-T-G
• gnomAD v4: 2-85545950-T-G
• COSMIC: COSN18004848
• MyVariant Identifiers: chr2:g.85773073T>G (hg19) ; chr2:g.85545950T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85545950T>G , CM000664.2:g.85545950T>G	GRCh38
NC_000002.11:g.85773073T>G , CM000664.1:g.85773073T>G	GRCh37
NC_000002.10:g.85626584T>G	NCBI36
NG_011811.2:g.20585A>C
NG_029183.1:g.11973T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000233838.9:c.*3984A>C MANE Select	ENSP00000233838.3:n.*3984A>C
ENST00000233838.8:c.*3984A>C	ENSP00000233838.3:n.*3984A>C
NM_000821.5:c.*3984A>C	NP_000812.2:n.*3984A>C
NM_000821.6:c.*3984A>C	NP_000812.2:n.*3984A>C
NM_001142269.2:c.*3984A>C	NP_001135741.1:n.*3984A>C
NM_001142269.3:c.*3984A>C	NP_001135741.1:n.*3984A>C
NM_000821.7:c.*3984A>C MANE Select	NP_000812.2:n.*3984A>C
NM_001142269.4:c.*3984A>C	NP_001135741.1:n.*3984A>C