Canonical Allele Identifier: CA403642042

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6713200C>G (hg19) ; chr19:g.6713189C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713189C>G , CM000681.2:g.6713189C>G	GRCh38
NC_000019.9:g.6713200C>G , CM000681.1:g.6713200C>G	GRCh37
NC_000019.8:g.6664200C>G	NCBI36
NG_009557.1:g.12463G>C , LRG_27:g.12463G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.880G>C	ENSP00000512083.1:p.Gly294Arg
ENST00000695654.1:c.127G>C	ENSP00000512085.1:p.Gly43Arg
ENST00000695692.1:n.327G>C
ENST00000245907.11:c.1003G>C MANE Select	ENSP00000245907.4:p.Gly335Arg
ENST00000245907.10:c.1003G>C	ENSP00000245907.4:p.Gly335Arg
ENST00000594270.5:n.127G>C
ENST00000595577.1:n.507G>C
ENST00000597442.5:n.253G>C
NM_000064.3:c.1003G>C	NP_000055.2:p.Gly335Arg
NM_000064.4:c.1003G>C MANE Select	NP_000055.2:p.Gly335Arg