Canonical Allele Identifier: CA505122368

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6682174T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6682163T>C , CM000681.2:g.6682163T>C	GRCh38
NC_000019.9:g.6682174T>C , CM000681.1:g.6682174T>C	GRCh37
NC_000019.8:g.6633174T>C	NCBI36
NG_009557.1:g.43489A>G , LRG_27:g.43489A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2587A>G
ENST00000695653.1:c.2148A>G	ENSP00000512084.1:p.Pro716=
ENST00000695654.1:c.3264A>G	ENSP00000512085.1:p.Pro1088=
ENST00000695689.1:c.210A>G	ENSP00000512101.1:n.210A>G
ENST00000695690.1:n.430A>G
ENST00000695691.1:n.430A>G
ENST00000245907.11:c.4239A>G MANE Select	ENSP00000245907.4:p.Pro1413=
ENST00000245907.10:c.4239A>G	ENSP00000245907.4:p.Pro1413=
ENST00000596548.1:c.360A>G	ENSP00000469744.1:p.Pro120=
ENST00000599899.5:n.1198A>G
ENST00000601008.1:c.242-4205A>G	ENSP00000471384.1:n.242-4205A>G
NM_000064.3:c.4239A>G	NP_000055.2:p.Pro1413=
NM_000064.4:c.4239A>G MANE Select	NP_000055.2:p.Pro1413=