Canonical Allele Identifier: CA403633025

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697477A>G (hg19) ; chr19:g.6697466A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697466A>G , CM000681.2:g.6697466A>G	GRCh38
NC_000019.9:g.6697477A>G , CM000681.1:g.6697477A>G	GRCh37
NC_000019.8:g.6648477A>G	NCBI36
NG_009557.1:g.28186T>C , LRG_27:g.28186T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1022T>C
ENST00000695652.1:c.2551T>C	ENSP00000512083.1:p.Ser851Pro
ENST00000695653.1:c.583T>C	ENSP00000512084.1:p.Ser195Pro
ENST00000695654.1:c.1798T>C	ENSP00000512085.1:p.Ser600Pro
ENST00000695655.1:c.1615T>C	ENSP00000512086.1:n.1615T>C
ENST00000695692.1:n.2038T>C
ENST00000245907.11:c.2674T>C MANE Select	ENSP00000245907.4:p.Ser892Pro
ENST00000245907.10:c.2674T>C	ENSP00000245907.4:p.Ser892Pro
ENST00000594005.1:n.250T>C
NM_000064.3:c.2674T>C	NP_000055.2:p.Ser892Pro
NM_000064.4:c.2674T>C MANE Select	NP_000055.2:p.Ser892Pro