Canonical Allele Identifier: CA1266819895
Gene: GGCX HGNC NCBI

Linked Data

dbSNP Id: rs1691636960
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85545864C>T , CM000664.2:g.85545864C>T GRCh38
NC_000002.11:g.85772987C>T , CM000664.1:g.85772987C>T GRCh37
NC_000002.10:g.85626498C>T NCBI36
NG_011811.2:g.20671G>A
NG_029183.1:g.11887C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000233838.9:c.*4070G>A MANE Select ENSP00000233838.3:n.*4070G>A
ENST00000233838.8:c.*4070G>A ENSP00000233838.3:n.*4070G>A
NM_000821.5:c.*4070G>A NP_000812.2:n.*4070G>A
NM_000821.6:c.*4070G>A NP_000812.2:n.*4070G>A
NM_001142269.2:c.*4070G>A NP_001135741.1:n.*4070G>A
NM_001142269.3:c.*4070G>A NP_001135741.1:n.*4070G>A
NM_000821.7:c.*4070G>A MANE Select NP_000812.2:n.*4070G>A
NM_001142269.4:c.*4070G>A NP_001135741.1:n.*4070G>A
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