Canonical Allele Identifier: CA403619925

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6686251C>A (hg19) ; chr19:g.6686240C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686240C>A , CM000681.2:g.6686240C>A	GRCh38
NC_000019.9:g.6686251C>A , CM000681.1:g.6686251C>A	GRCh37
NC_000019.8:g.6637251C>A	NCBI36
NG_009557.1:g.39412G>T , LRG_27:g.39412G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2042G>T
ENST00000695652.1:c.3571G>T	ENSP00000512083.1:p.Ala1191Ser
ENST00000695653.1:c.1603G>T	ENSP00000512084.1:p.Ala535Ser
ENST00000695654.1:c.2719G>T	ENSP00000512085.1:p.Ala907Ser
ENST00000695655.1:c.2635G>T	ENSP00000512086.1:n.2635G>T
ENST00000695692.1:n.3058G>T
ENST00000245907.11:c.3694G>T MANE Select	ENSP00000245907.4:p.Ala1232Ser
ENST00000245907.10:c.3694G>T	ENSP00000245907.4:p.Ala1232Ser
ENST00000596238.1:n.137G>T
ENST00000601008.1:c.241+506G>T	ENSP00000471384.1:n.241+506G>T
NM_000064.3:c.3694G>T	NP_000055.2:p.Ala1232Ser
NM_000064.4:c.3694G>T MANE Select	NP_000055.2:p.Ala1232Ser