Canonical Allele Identifier: CA505193033

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6713261G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713250G>C , CM000681.2:g.6713250G>C	GRCh38
NC_000019.9:g.6713261G>C , CM000681.1:g.6713261G>C	GRCh37
NC_000019.8:g.6664261G>C	NCBI36
NG_009557.1:g.12402C>G , LRG_27:g.12402C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.819C>G	ENSP00000512083.1:p.Pro273=
ENST00000695654.1:c.66C>G	ENSP00000512085.1:p.Pro22=
ENST00000695692.1:n.266C>G
ENST00000245907.11:c.942C>G MANE Select	ENSP00000245907.4:p.Pro314=
ENST00000245907.10:c.942C>G	ENSP00000245907.4:p.Pro314=
ENST00000594270.5:n.66C>G
ENST00000595577.1:n.446C>G
ENST00000597442.5:n.192C>G
NM_000064.3:c.942C>G	NP_000055.2:p.Pro314=
NM_000064.4:c.942C>G MANE Select	NP_000055.2:p.Pro314=