Canonical Allele Identifier: CA403642785

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6713507T>G (hg19) ; chr19:g.6713496T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713496T>G , CM000681.2:g.6713496T>G	GRCh38
NC_000019.9:g.6713507T>G , CM000681.1:g.6713507T>G	GRCh37
NC_000019.8:g.6664507T>G	NCBI36
NG_009557.1:g.12156A>C , LRG_27:g.12156A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.664A>C	ENSP00000512083.1:p.Lys222Gln
ENST00000695692.1:n.111A>C
ENST00000245907.11:c.787A>C MANE Select	ENSP00000245907.4:p.Lys263Gln
ENST00000245907.10:c.787A>C	ENSP00000245907.4:p.Lys263Gln
ENST00000595577.1:n.291A>C
ENST00000597442.5:n.37A>C
NM_000064.3:c.787A>C	NP_000055.2:p.Lys263Gln
NM_000064.4:c.787A>C MANE Select	NP_000055.2:p.Lys263Gln