Canonical Allele Identifier: CA505192548

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697747C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697736C>G , CM000681.2:g.6697736C>G	GRCh38
NC_000019.9:g.6697747C>G , CM000681.1:g.6697747C>G	GRCh37
NC_000019.8:g.6648747C>G	NCBI36
NG_009557.1:g.27916G>C , LRG_27:g.27916G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.847G>C
ENST00000695652.1:c.2376G>C	ENSP00000512083.1:p.Leu792=
ENST00000695653.1:c.408G>C	ENSP00000512084.1:p.Leu136=
ENST00000695654.1:c.1623G>C	ENSP00000512085.1:p.Leu541=
ENST00000695655.1:c.1440G>C	ENSP00000512086.1:n.1440G>C
ENST00000695692.1:n.1863G>C
ENST00000245907.11:c.2499G>C MANE Select	ENSP00000245907.4:p.Leu833=
ENST00000245907.10:c.2499G>C	ENSP00000245907.4:p.Leu833=
ENST00000602053.1:n.547G>C
NM_000064.3:c.2499G>C	NP_000055.2:p.Leu833=
NM_000064.4:c.2499G>C MANE Select	NP_000055.2:p.Leu833=