Canonical Allele Identifier: CA403619870

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6686239C>A (hg19) ; chr19:g.6686228C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686228C>A , CM000681.2:g.6686228C>A	GRCh38
NC_000019.9:g.6686239C>A , CM000681.1:g.6686239C>A	GRCh37
NC_000019.8:g.6637239C>A	NCBI36
NG_009557.1:g.39424G>T , LRG_27:g.39424G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2054G>T
ENST00000695652.1:c.3583G>T	ENSP00000512083.1:p.Ala1195Ser
ENST00000695653.1:c.1615G>T	ENSP00000512084.1:p.Ala539Ser
ENST00000695654.1:c.2731G>T	ENSP00000512085.1:p.Ala911Ser
ENST00000695655.1:c.2647G>T	ENSP00000512086.1:n.2647G>T
ENST00000695692.1:n.3070G>T
ENST00000245907.11:c.3706G>T MANE Select	ENSP00000245907.4:p.Ala1236Ser
ENST00000245907.10:c.3706G>T	ENSP00000245907.4:p.Ala1236Ser
ENST00000596238.1:n.149G>T
ENST00000601008.1:c.241+518G>T	ENSP00000471384.1:n.241+518G>T
NM_000064.3:c.3706G>T	NP_000055.2:p.Ala1236Ser
NM_000064.4:c.3706G>T MANE Select	NP_000055.2:p.Ala1236Ser