Canonical Allele Identifier: CA505125002

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6714238T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6714227T>A , CM000681.2:g.6714227T>A	GRCh38
NC_000019.9:g.6714238T>A , CM000681.1:g.6714238T>A	GRCh37
NC_000019.8:g.6665238T>A	NCBI36
NG_009557.1:g.11425A>T , LRG_27:g.11425A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.498A>T	ENSP00000512083.1:p.Arg166=
ENST00000245907.11:c.621A>T MANE Select	ENSP00000245907.4:p.Arg207=
ENST00000245907.10:c.621A>T	ENSP00000245907.4:p.Arg207=
ENST00000595577.1:n.125A>T
NM_000064.3:c.621A>T	NP_000055.2:p.Arg207=
NM_000064.4:c.621A>T MANE Select	NP_000055.2:p.Arg207=