Canonical Allele Identifier: CA427440051
Gene: GGCX HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.85780373A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85553250A>G , CM000664.2:g.85553250A>G GRCh38
NC_000002.11:g.85780373A>G , CM000664.1:g.85780373A>G GRCh37
NC_000002.10:g.85633884A>G NCBI36
NG_011811.2:g.13285T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000473665.2:n.5181T>C
ENST00000482662.2:n.3588T>C
ENST00000685865.1:n.1540T>C
ENST00000687250.1:n.1240T>C
ENST00000687995.1:n.1489T>C
ENST00000688205.1:c.*730T>C ENSP00000509673.1:n.*730T>C
ENST00000688788.1:n.1376T>C
ENST00000689276.1:c.1068T>C ENSP00000510012.1:p.Tyr356=
ENST00000689576.1:c.1137T>C ENSP00000508712.1:p.Tyr379=
ENST00000690108.1:c.*793T>C ENSP00000510617.1:n.*793T>C
ENST00000690468.1:c.858T>C ENSP00000509078.1:p.Tyr286=
ENST00000690595.1:c.462T>C ENSP00000508979.1:p.Tyr154=
ENST00000691348.1:c.966T>C ENSP00000509369.1:p.Tyr322=
ENST00000691410.1:c.*714T>C ENSP00000508479.1:n.*714T>C
ENST00000693287.1:c.453T>C ENSP00000510264.1:p.Tyr151=
ENST00000693681.1:c.450T>C ENSP00000510789.1:p.Tyr150=
ENST00000233838.9:c.1137T>C MANE Select ENSP00000233838.3:p.Tyr379=
ENST00000233838.8:c.1137T>C ENSP00000233838.3:p.Tyr379=
ENST00000430215.7:c.966T>C ENSP00000408045.3:p.Tyr322=
ENST00000465637.5:n.179-5246T>C
ENST00000473665.1:n.630T>C
ENST00000482662.1:n.554T>C
NM_000821.5:c.1137T>C NP_000812.2:p.Tyr379=
NM_000821.6:c.1137T>C NP_000812.2:p.Tyr379=
NM_001142269.2:c.966T>C NP_001135741.1:p.Tyr322=
NM_001142269.3:c.966T>C NP_001135741.1:p.Tyr322=
XM_005264259.3:c.1137T>C XP_005264316.1:p.Tyr379=
XM_011532764.1:c.315T>C XP_011531066.1:p.Tyr105=
XM_011532765.1:c.315T>C XP_011531067.1:p.Tyr105=
XR_939677.1:n.1202T>C
XM_005264259.5:c.1137T>C XP_005264316.1:p.Tyr379=
XM_011532764.3:c.315T>C XP_011531066.1:p.Tyr105=
XM_011532765.3:c.315T>C XP_011531067.1:p.Tyr105=
XM_017003803.2:c.966T>C XP_016859292.1:p.Tyr322=
XR_001738703.2:n.1202T>C
NM_000821.7:c.1137T>C MANE Select NP_000812.2:p.Tyr379=
NM_001142269.4:c.966T>C NP_001135741.1:p.Tyr322=