Canonical Allele Identifier: CA1266820805
Gene: GGCX HGNC NCBI

Linked Data

dbSNP Id: rs1691670069
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85546426G>A , CM000664.2:g.85546426G>A GRCh38
NC_000002.11:g.85773549G>A , CM000664.1:g.85773549G>A GRCh37
NC_000002.10:g.85627060G>A NCBI36
NG_011811.2:g.20109C>T
NG_029183.1:g.12449G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000233838.9:c.*3508C>T MANE Select ENSP00000233838.3:n.*3508C>T
ENST00000233838.8:c.*3508C>T ENSP00000233838.3:n.*3508C>T
NM_000821.5:c.*3508C>T NP_000812.2:n.*3508C>T
NM_000821.6:c.*3508C>T NP_000812.2:n.*3508C>T
NM_001142269.2:c.*3508C>T NP_001135741.1:n.*3508C>T
NM_001142269.3:c.*3508C>T NP_001135741.1:n.*3508C>T
NM_000821.7:c.*3508C>T MANE Select NP_000812.2:n.*3508C>T
NM_001142269.4:c.*3508C>T NP_001135741.1:n.*3508C>T
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