Canonical Allele Identifier: CA894034811

Gene: GGCX

Linked Data

• dbSNP Id: rs1179191922
• gnomAD v3: 2-85546412-G-A
• gnomAD v4: 2-85546412-G-A
• MyVariant Identifiers: chr2:g.85773535G>A (hg19) ; chr2:g.85546412G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85546412G>A , CM000664.2:g.85546412G>A	GRCh38
NC_000002.11:g.85773535G>A , CM000664.1:g.85773535G>A	GRCh37
NC_000002.10:g.85627046G>A	NCBI36
NG_011811.2:g.20123C>T
NG_029183.1:g.12435G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000233838.9:c.*3522C>T MANE Select	ENSP00000233838.3:n.*3522C>T
ENST00000233838.8:c.*3522C>T	ENSP00000233838.3:n.*3522C>T
NM_000821.5:c.*3522C>T	NP_000812.2:n.*3522C>T
NM_000821.6:c.*3522C>T	NP_000812.2:n.*3522C>T
NM_001142269.2:c.*3522C>T	NP_001135741.1:n.*3522C>T
NM_001142269.3:c.*3522C>T	NP_001135741.1:n.*3522C>T
NM_000821.7:c.*3522C>T MANE Select	NP_000812.2:n.*3522C>T
NM_001142269.4:c.*3522C>T	NP_001135741.1:n.*3522C>T