Canonical Allele Identifier: CA2587876918

Gene: C3

Linked Data

• gnomAD v4: 19-6709588-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709588C>A , CM000681.2:g.6709588C>A	GRCh38
NC_000019.9:g.6709599C>A , CM000681.1:g.6709599C>A	GRCh37
NC_000019.8:g.6660599C>A	NCBI36
NG_009557.1:g.16064G>T , LRG_27:g.16064G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000695652.1:c.1722+96G>T	ENSP00000512083.1:n.1722+96G>T
ENST00000695654.1:c.969+96G>T	ENSP00000512085.1:n.969+96G>T
ENST00000695655.1:c.786+96G>T	ENSP00000512086.1:n.786+96G>T
ENST00000695692.1:n.1209+96G>T
ENST00000245907.11:c.1845+96G>T MANE Select	ENSP00000245907.4:n.1845+96G>T
ENST00000245907.10:c.1845+96G>T	ENSP00000245907.4:n.1845+96G>T
NM_000064.3:c.1845+96G>T	NP_000055.2:n.1845+96G>T
NM_000064.4:c.1845+96G>T MANE Select	NP_000055.2:n.1845+96G>T