Canonical Allele Identifier: CA403633001

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697468A>T (hg19) ; chr19:g.6697457A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697457A>T , CM000681.2:g.6697457A>T	GRCh38
NC_000019.9:g.6697468A>T , CM000681.1:g.6697468A>T	GRCh37
NC_000019.8:g.6648468A>T	NCBI36
NG_009557.1:g.28195T>A , LRG_27:g.28195T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1031T>A
ENST00000695652.1:c.2560T>A	ENSP00000512083.1:p.Ser854Thr
ENST00000695653.1:c.592T>A	ENSP00000512084.1:p.Ser198Thr
ENST00000695654.1:c.1807T>A	ENSP00000512085.1:p.Ser603Thr
ENST00000695655.1:c.1624T>A	ENSP00000512086.1:n.1624T>A
ENST00000695692.1:n.2047T>A
ENST00000245907.11:c.2683T>A MANE Select	ENSP00000245907.4:p.Ser895Thr
ENST00000245907.10:c.2683T>A	ENSP00000245907.4:p.Ser895Thr
ENST00000594005.1:n.259T>A
NM_000064.3:c.2683T>A	NP_000055.2:p.Ser895Thr
NM_000064.4:c.2683T>A MANE Select	NP_000055.2:p.Ser895Thr