Canonical Allele Identifier: CA1266822748
Gene: GGCX HGNC NCBI

Linked Data

dbSNP Id: rs1573314717
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85547900G>A , CM000664.2:g.85547900G>A GRCh38
NC_000002.11:g.85775023G>A , CM000664.1:g.85775023G>A GRCh37
NC_000002.10:g.85628534G>A NCBI36
NG_011811.2:g.18635C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000233838.9:c.*2034C>T MANE Select ENSP00000233838.3:n.*2034C>T
ENST00000233838.8:c.*2034C>T ENSP00000233838.3:n.*2034C>T
ENST00000465637.5:n.283C>T
NM_000821.5:c.*2034C>T NP_000812.2:n.*2034C>T
NM_000821.6:c.*2034C>T NP_000812.2:n.*2034C>T
NM_001142269.2:c.*2034C>T NP_001135741.1:n.*2034C>T
NM_001142269.3:c.*2034C>T NP_001135741.1:n.*2034C>T
NM_000821.7:c.*2034C>T MANE Select NP_000812.2:n.*2034C>T
NM_001142269.4:c.*2034C>T NP_001135741.1:n.*2034C>T
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