Canonical Allele Identifier: CA1266819755
Gene: GGCX HGNC NCBI

Linked Data

dbSNP Id: rs369547539
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85545744G>T , CM000664.2:g.85545744G>T GRCh38
NC_000002.11:g.85772867G>T , CM000664.1:g.85772867G>T GRCh37
NC_000002.10:g.85626378G>T NCBI36
NG_011811.2:g.20791C>A
NG_029183.1:g.11767G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000233838.9:c.*4190C>A MANE Select ENSP00000233838.3:n.*4190C>A
ENST00000233838.8:c.*4190C>A ENSP00000233838.3:n.*4190C>A
NM_000821.5:c.*4190C>A NP_000812.2:n.*4190C>A
NM_000821.6:c.*4190C>A NP_000812.2:n.*4190C>A
NM_001142269.2:c.*4190C>A NP_001135741.1:n.*4190C>A
NM_001142269.3:c.*4190C>A NP_001135741.1:n.*4190C>A
NM_000821.7:c.*4190C>A MANE Select NP_000812.2:n.*4190C>A
NM_001142269.4:c.*4190C>A NP_001135741.1:n.*4190C>A
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