Canonical Allele Identifier: CA9129067

Gene: C3

Linked Data

• dbSNP Id: rs772231766
• ExAC: 19:6697836 C / A
• gnomAD v2: 19-6697836-C-A
• gnomAD v3: 19-6697825-C-A
• gnomAD v4: 19-6697825-C-A
• MyVariant Identifiers: chr19:g.6697836C>A (hg19) ; chr19:g.6697825C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697825C>A , CM000681.2:g.6697825C>A	GRCh38
NC_000019.9:g.6697836C>A , CM000681.1:g.6697836C>A	GRCh37
NC_000019.8:g.6648836C>A	NCBI36
NG_009557.1:g.27827G>T , LRG_27:g.27827G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000695651.1:n.789-31G>T
ENST00000695652.1:c.2318-31G>T	ENSP00000512083.1:n.2318-31G>T
ENST00000695653.1:c.350-31G>T	ENSP00000512084.1:n.350-31G>T
ENST00000695654.1:c.1565-31G>T	ENSP00000512085.1:n.1565-31G>T
ENST00000695655.1:c.1382-31G>T	ENSP00000512086.1:n.1382-31G>T
ENST00000695692.1:n.1805-31G>T
ENST00000245907.11:c.2441-31G>T MANE Select	ENSP00000245907.4:n.2441-31G>T
ENST00000245907.10:c.2441-31G>T	ENSP00000245907.4:n.2441-31G>T
ENST00000602053.1:n.489-31G>T
NM_000064.3:c.2441-31G>T	NP_000055.2:n.2441-31G>T
NM_000064.4:c.2441-31G>T MANE Select	NP_000055.2:n.2441-31G>T