Canonical Allele Identifier: CA2571570934

Gene: GGCX

Linked Data

• dbSNP Id: rs2103930282
• gnomAD v3: 2-85545893-G-A
• gnomAD v4: 2-85545893-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85545893G>A , CM000664.2:g.85545893G>A	GRCh38
NC_000002.11:g.85773016G>A , CM000664.1:g.85773016G>A	GRCh37
NC_000002.10:g.85626527G>A	NCBI36
NG_011811.2:g.20642C>T
NG_029183.1:g.11916G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233838.9:c.*4041C>T MANE Select	ENSP00000233838.3:n.*4041C>T
ENST00000233838.8:c.*4041C>T	ENSP00000233838.3:n.*4041C>T
NM_000821.5:c.*4041C>T	NP_000812.2:n.*4041C>T
NM_000821.6:c.*4041C>T	NP_000812.2:n.*4041C>T
NM_001142269.2:c.*4041C>T	NP_001135741.1:n.*4041C>T
NM_001142269.3:c.*4041C>T	NP_001135741.1:n.*4041C>T
NM_000821.7:c.*4041C>T MANE Select	NP_000812.2:n.*4041C>T
NM_001142269.4:c.*4041C>T	NP_001135741.1:n.*4041C>T