Canonical Allele Identifier: CA2587875603

Gene: C3

Linked Data

• gnomAD v4: 19-6697629-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697629G>A , CM000681.2:g.6697629G>A	GRCh38
NC_000019.9:g.6697640G>A , CM000681.1:g.6697640G>A	GRCh37
NC_000019.8:g.6648640G>A	NCBI36
NG_009557.1:g.28023C>T , LRG_27:g.28023C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.931+23C>T
ENST00000695652.1:c.2460+23C>T	ENSP00000512083.1:n.2460+23C>T
ENST00000695653.1:c.492+23C>T	ENSP00000512084.1:n.492+23C>T
ENST00000695654.1:c.1707+23C>T	ENSP00000512085.1:n.1707+23C>T
ENST00000695655.1:c.1524+23C>T	ENSP00000512086.1:n.1524+23C>T
ENST00000695692.1:n.1947+23C>T
ENST00000245907.11:c.2583+23C>T MANE Select	ENSP00000245907.4:n.2583+23C>T
ENST00000245907.10:c.2583+23C>T	ENSP00000245907.4:n.2583+23C>T
ENST00000594005.1:n.87C>T
NM_000064.3:c.2583+23C>T	NP_000055.2:n.2583+23C>T
NM_000064.4:c.2583+23C>T MANE Select	NP_000055.2:n.2583+23C>T