Canonical Allele Identifier: CA51729756

Gene: GGCX

Linked Data

• dbSNP Id: rs988799010
• MyVariant Identifiers: chr2:g.85773717C>G (hg19) ; chr2:g.85546594C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85546594C>G , CM000664.2:g.85546594C>G	GRCh38
NC_000002.11:g.85773717C>G , CM000664.1:g.85773717C>G	GRCh37
NC_000002.10:g.85627228C>G	NCBI36
NG_011811.2:g.19941G>C
NG_029183.1:g.12617C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233838.9:c.*3340G>C MANE Select	ENSP00000233838.3:n.*3340G>C
ENST00000233838.8:c.*3340G>C	ENSP00000233838.3:n.*3340G>C
NM_000821.5:c.*3340G>C	NP_000812.2:n.*3340G>C
NM_000821.6:c.*3340G>C	NP_000812.2:n.*3340G>C
NM_001142269.2:c.*3340G>C	NP_001135741.1:n.*3340G>C
NM_001142269.3:c.*3340G>C	NP_001135741.1:n.*3340G>C
NM_000821.7:c.*3340G>C MANE Select	NP_000812.2:n.*3340G>C
NM_001142269.4:c.*3340G>C	NP_001135741.1:n.*3340G>C