Canonical Allele Identifier: CA1033077968
Gene: GGCX HGNC NCBI

Linked Data

dbSNP Id: rs1691662202
gnomAD v3: 2-85546320-G-C
gnomAD v4: 2-85546320-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85546320G>C , CM000664.2:g.85546320G>C GRCh38
NC_000002.11:g.85773443G>C , CM000664.1:g.85773443G>C GRCh37
NC_000002.10:g.85626954G>C NCBI36
NG_011811.2:g.20215C>G
NG_029183.1:g.12343G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000233838.9:c.*3614C>G MANE Select ENSP00000233838.3:n.*3614C>G
ENST00000233838.8:c.*3614C>G ENSP00000233838.3:n.*3614C>G
NM_000821.5:c.*3614C>G NP_000812.2:n.*3614C>G
NM_000821.6:c.*3614C>G NP_000812.2:n.*3614C>G
NM_001142269.2:c.*3614C>G NP_001135741.1:n.*3614C>G
NM_001142269.3:c.*3614C>G NP_001135741.1:n.*3614C>G
NM_000821.7:c.*3614C>G MANE Select NP_000812.2:n.*3614C>G
NM_001142269.4:c.*3614C>G NP_001135741.1:n.*3614C>G