Canonical Allele Identifier: CA2750761378
Gene: GGCX HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85546424A>G , CM000664.2:g.85546424A>G GRCh38
NC_000002.11:g.85773547A>G , CM000664.1:g.85773547A>G GRCh37
NC_000002.10:g.85627058A>G NCBI36
NG_011811.2:g.20111T>C
NG_029183.1:g.12447A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000233838.9:c.*3510T>C MANE Select ENSP00000233838.3:n.*3510T>C
ENST00000233838.8:c.*3510T>C ENSP00000233838.3:n.*3510T>C
NM_000821.5:c.*3510T>C NP_000812.2:n.*3510T>C
NM_000821.6:c.*3510T>C NP_000812.2:n.*3510T>C
NM_001142269.2:c.*3510T>C NP_001135741.1:n.*3510T>C
NM_001142269.3:c.*3510T>C NP_001135741.1:n.*3510T>C
NM_000821.7:c.*3510T>C MANE Select NP_000812.2:n.*3510T>C
NM_001142269.4:c.*3510T>C NP_001135741.1:n.*3510T>C
Search 100 bp 5'
Search 100 bp 3'