Canonical Allele Identifier: CA347491957

Gene: GGCX

Linked Data

• dbSNP Id: rs1367986537
• gnomAD v2: 2-85786046-A-G
• gnomAD v4: 2-85558923-A-G
• MyVariant Identifiers: chr2:g.85786046A>G (hg19) ; chr2:g.85558923A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85558923A>G , CM000664.2:g.85558923A>G	GRCh38
NC_000002.11:g.85786046A>G , CM000664.1:g.85786046A>G	GRCh37
NC_000002.10:g.85639557A>G	NCBI36
NG_011811.2:g.7612T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.153T>C
ENST00000482662.2:n.411+23T>C
ENST00000496962.2:c.367T>C	ENSP00000508856.1:p.Phe123Leu
ENST00000685865.1:n.459T>C
ENST00000687250.1:n.470T>C
ENST00000687995.1:n.408T>C
ENST00000688205.1:c.367T>C	ENSP00000509673.1:p.Phe123Leu
ENST00000688788.1:n.459T>C
ENST00000689276.1:c.344+23T>C	ENSP00000510012.1:n.344+23T>C
ENST00000689576.1:c.367T>C	ENSP00000508712.1:p.Phe123Leu
ENST00000690108.1:c.344+23T>C	ENSP00000510617.1:n.344+23T>C
ENST00000690468.1:c.173+23T>C	ENSP00000509078.1:n.173+23T>C
ENST00000690595.1:c.214+1892T>C	ENSP00000508979.1:n.214+1892T>C
ENST00000691348.1:c.196T>C	ENSP00000509369.1:p.Phe66Leu
ENST00000691410.1:c.344+23T>C	ENSP00000508479.1:n.344+23T>C
ENST00000693287.1:c.-67+2463T>C	ENSP00000510264.1:n.-67+2463T>C
ENST00000693681.1:c.196T>C	ENSP00000510789.1:p.Phe66Leu
ENST00000233838.9:c.367T>C MANE Select	ENSP00000233838.3:p.Phe123Leu
ENST00000233838.8:c.367T>C	ENSP00000233838.3:p.Phe123Leu
ENST00000421496.5:c.173+23T>C	ENSP00000400384.1:n.173+23T>C
ENST00000423570.5:c.344+23T>C	ENSP00000389426.1:n.344+23T>C
ENST00000428479.3:c.196T>C	ENSP00000390748.3:p.Phe66Leu
ENST00000430215.7:c.196T>C	ENSP00000408045.3:p.Phe66Leu
ENST00000465637.5:n.178+83T>C
ENST00000481541.1:n.261T>C
ENST00000496962.1:n.486T>C
NM_000821.5:c.367T>C	NP_000812.2:p.Phe123Leu
NM_000821.6:c.367T>C	NP_000812.2:p.Phe123Leu
NM_001142269.2:c.196T>C	NP_001135741.1:p.Phe66Leu
NM_001142269.3:c.196T>C	NP_001135741.1:p.Phe66Leu
NM_001311312.1:c.367T>C	NP_001298241.1:p.Phe123Leu
XM_005264259.3:c.367T>C	XP_005264316.1:p.Phe123Leu
XM_011532764.1:c.-292T>C	XP_011531066.1:n.-292T>C
XM_011532765.1:c.-292T>C	XP_011531067.1:n.-292T>C
XR_939677.1:n.432T>C
XM_005264259.5:c.367T>C	XP_005264316.1:p.Phe123Leu
XM_011532764.3:c.-292T>C	XP_011531066.1:n.-292T>C
XM_011532765.3:c.-292T>C	XP_011531067.1:n.-292T>C
XM_017003803.2:c.196T>C	XP_016859292.1:p.Phe66Leu
XR_001738703.2:n.432T>C
NM_000821.7:c.367T>C MANE Select	NP_000812.2:p.Phe123Leu
NM_001142269.4:c.196T>C	NP_001135741.1:p.Phe66Leu
NM_001311312.2:c.367T>C	NP_001298241.1:p.Phe123Leu