Canonical Allele Identifier: CA505125004

Gene: C3

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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