Canonical Allele Identifier: CA2659852273
Gene: GGCX HGNC NCBI

Linked Data

gnomAD v4: 2-85545861-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85545861T>C , CM000664.2:g.85545861T>C GRCh38
NC_000002.11:g.85772984T>C , CM000664.1:g.85772984T>C GRCh37
NC_000002.10:g.85626495T>C NCBI36
NG_011811.2:g.20674A>G
NG_029183.1:g.11884T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000233838.9:c.*4073A>G MANE Select ENSP00000233838.3:n.*4073A>G
ENST00000233838.8:c.*4073A>G ENSP00000233838.3:n.*4073A>G
NM_000821.5:c.*4073A>G NP_000812.2:n.*4073A>G
NM_000821.6:c.*4073A>G NP_000812.2:n.*4073A>G
NM_001142269.2:c.*4073A>G NP_001135741.1:n.*4073A>G
NM_001142269.3:c.*4073A>G NP_001135741.1:n.*4073A>G
NM_000821.7:c.*4073A>G MANE Select NP_000812.2:n.*4073A>G
NM_001142269.4:c.*4073A>G NP_001135741.1:n.*4073A>G