Canonical Allele Identifier: CA2587875484

Gene: C3

Linked Data

• gnomAD v4: 19-6697896-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697896A>T , CM000681.2:g.6697896A>T	GRCh38
NC_000019.9:g.6697907A>T , CM000681.1:g.6697907A>T	GRCh37
NC_000019.8:g.6648907A>T	NCBI36
NG_009557.1:g.27756T>A , LRG_27:g.27756T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.789-102T>A
ENST00000695652.1:c.2318-102T>A	ENSP00000512083.1:n.2318-102T>A
ENST00000695653.1:c.350-102T>A	ENSP00000512084.1:n.350-102T>A
ENST00000695654.1:c.1565-102T>A	ENSP00000512085.1:n.1565-102T>A
ENST00000695655.1:c.1382-102T>A	ENSP00000512086.1:n.1382-102T>A
ENST00000695692.1:n.1805-102T>A
ENST00000245907.11:c.2441-102T>A MANE Select	ENSP00000245907.4:n.2441-102T>A
ENST00000245907.10:c.2441-102T>A	ENSP00000245907.4:n.2441-102T>A
ENST00000602053.1:n.489-102T>A
NM_000064.3:c.2441-102T>A	NP_000055.2:n.2441-102T>A
NM_000064.4:c.2441-102T>A MANE Select	NP_000055.2:n.2441-102T>A