Canonical Allele Identifier: CA51730813
Gene: GGCX HGNC NCBI

Linked Data

dbSNP Id: rs982921732
MyVariant Identifiers: chr2:g.85775009T>G (hg19) chr2:g.85547886T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85547886T>G , CM000664.2:g.85547886T>G GRCh38
NC_000002.11:g.85775009T>G , CM000664.1:g.85775009T>G GRCh37
NC_000002.10:g.85628520T>G NCBI36
NG_011811.2:g.18649A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000233838.9:c.*2048A>C MANE Select ENSP00000233838.3:n.*2048A>C
ENST00000233838.8:c.*2048A>C ENSP00000233838.3:n.*2048A>C
ENST00000465637.5:n.297A>C
NM_000821.5:c.*2048A>C NP_000812.2:n.*2048A>C
NM_000821.6:c.*2048A>C NP_000812.2:n.*2048A>C
NM_001142269.2:c.*2048A>C NP_001135741.1:n.*2048A>C
NM_001142269.3:c.*2048A>C NP_001135741.1:n.*2048A>C
NM_000821.7:c.*2048A>C MANE Select NP_000812.2:n.*2048A>C
NM_001142269.4:c.*2048A>C NP_001135741.1:n.*2048A>C
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