Canonical Allele Identifier: CA505124963

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6714086G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6714075G>C , CM000681.2:g.6714075G>C	GRCh38
NC_000019.9:g.6714086G>C , CM000681.1:g.6714086G>C	GRCh37
NC_000019.8:g.6665086G>C	NCBI36
NG_009557.1:g.11577C>G , LRG_27:g.11577C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.567C>G	ENSP00000512083.1:p.Pro189=
ENST00000245907.11:c.690C>G MANE Select	ENSP00000245907.4:p.Pro230=
ENST00000245907.10:c.690C>G	ENSP00000245907.4:p.Pro230=
ENST00000595577.1:n.194C>G
NM_000064.3:c.690C>G	NP_000055.2:p.Pro230=
NM_000064.4:c.690C>G MANE Select	NP_000055.2:p.Pro230=