Canonical Allele Identifier: CA2699793040
Gene: GGCX HGNC NCBI

Linked Data

dbSNP Id: rs1691674048
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85546508C>G , CM000664.2:g.85546508C>G GRCh38
NC_000002.11:g.85773631C>G , CM000664.1:g.85773631C>G GRCh37
NC_000002.10:g.85627142C>G NCBI36
NG_011811.2:g.20027G>C
NG_029183.1:g.12531C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000233838.9:c.*3426G>C MANE Select ENSP00000233838.3:n.*3426G>C
ENST00000233838.8:c.*3426G>C ENSP00000233838.3:n.*3426G>C
NM_000821.5:c.*3426G>C NP_000812.2:n.*3426G>C
NM_000821.6:c.*3426G>C NP_000812.2:n.*3426G>C
NM_001142269.2:c.*3426G>C NP_001135741.1:n.*3426G>C
NM_001142269.3:c.*3426G>C NP_001135741.1:n.*3426G>C
NM_000821.7:c.*3426G>C MANE Select NP_000812.2:n.*3426G>C
NM_001142269.4:c.*3426G>C NP_001135741.1:n.*3426G>C
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