Canonical Allele Identifier: CA330574850

Gene: VSIG4

Linked Data

• dbSNP Id: rs946222299
• gnomAD v3: X-66021931-T-C
• gnomAD v4: X-66021931-T-C
• MyVariant Identifiers: chrX:g.65241773T>C (hg19) ; chrX:g.66021931T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.66021931T>C , CM000685.2:g.66021931T>C	GRCh38
NC_000023.10:g.65241773T>C , CM000685.1:g.65241773T>C	GRCh37
NC_000023.9:g.65158498T>C	NCBI36
NG_021306.1:g.23195A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000374737.9:c.*332A>G MANE Select	ENSP00000363869.4:n.*332A>G
ENST00000651578.1:c.*782A>G	ENSP00000498502.1:n.*782A>G
ENST00000374737.8:c.*332A>G	ENSP00000363869.4:n.*332A>G
ENST00000412866.2:c.*332A>G	ENSP00000394143.2:n.*332A>G
ENST00000427538.5:c.977A>G
ENST00000455586.6:c.*906A>G	ENSP00000411581.2:n.*906A>G
NM_001100431.1:c.*332A>G	NP_001093901.1:n.*332A>G
NM_001184830.1:c.*906A>G	NP_001171759.1:n.*906A>G
NM_001184831.1:c.*906A>G	NP_001171760.1:n.*906A>G
NM_001257403.1:c.*154A>G	NP_001244332.1:n.*154A>G
NM_007268.2:c.*332A>G	NP_009199.1:n.*332A>G
XM_017029251.2:c.*154A>G	XP_016884740.1:n.*154A>G
NM_007268.3:c.*332A>G MANE Select	NP_009199.1:n.*332A>G
NM_001100431.2:c.*332A>G	NP_001093901.1:n.*332A>G
NM_001184831.2:c.*906A>G	NP_001171760.1:n.*906A>G
NM_001257403.2:c.*154A>G	NP_001244332.1:n.*154A>G
NM_001184830.2:c.*906A>G	NP_001171759.1:n.*906A>G