Canonical Allele Identifier: CA2587875546

Gene: C3

Linked Data

• gnomAD v4: 19-6697600-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697600G>A , CM000681.2:g.6697600G>A	GRCh38
NC_000019.9:g.6697611G>A , CM000681.1:g.6697611G>A	GRCh37
NC_000019.8:g.6648611G>A	NCBI36
NG_009557.1:g.28052C>T , LRG_27:g.28052C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.932-44C>T
ENST00000695652.1:c.2461-44C>T	ENSP00000512083.1:n.2461-44C>T
ENST00000695653.1:c.493-44C>T	ENSP00000512084.1:n.493-44C>T
ENST00000695654.1:c.1708-44C>T	ENSP00000512085.1:n.1708-44C>T
ENST00000695655.1:c.1525-44C>T	ENSP00000512086.1:n.1525-44C>T
ENST00000695692.1:n.1948-44C>T
ENST00000245907.11:c.2584-44C>T MANE Select	ENSP00000245907.4:n.2584-44C>T
ENST00000245907.10:c.2584-44C>T	ENSP00000245907.4:n.2584-44C>T
ENST00000594005.1:n.116C>T
NM_000064.3:c.2584-44C>T	NP_000055.2:n.2584-44C>T
NM_000064.4:c.2584-44C>T MANE Select	NP_000055.2:n.2584-44C>T