Canonical Allele Identifier: CA2659853403
Gene: GGCX HGNC NCBI

Linked Data

gnomAD v4: 2-85547888-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85547888C>A , CM000664.2:g.85547888C>A GRCh38
NC_000002.11:g.85775011C>A , CM000664.1:g.85775011C>A GRCh37
NC_000002.10:g.85628522C>A NCBI36
NG_011811.2:g.18647G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000233838.9:c.*2046G>T MANE Select ENSP00000233838.3:n.*2046G>T
ENST00000233838.8:c.*2046G>T ENSP00000233838.3:n.*2046G>T
ENST00000465637.5:n.295G>T
NM_000821.5:c.*2046G>T NP_000812.2:n.*2046G>T
NM_000821.6:c.*2046G>T NP_000812.2:n.*2046G>T
NM_001142269.2:c.*2046G>T NP_001135741.1:n.*2046G>T
NM_001142269.3:c.*2046G>T NP_001135741.1:n.*2046G>T
NM_000821.7:c.*2046G>T MANE Select NP_000812.2:n.*2046G>T
NM_001142269.4:c.*2046G>T NP_001135741.1:n.*2046G>T
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