Canonical Allele Identifier: CA403632720

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697401T>G (hg19) ; chr19:g.6697390T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697390T>G , CM000681.2:g.6697390T>G	GRCh38
NC_000019.9:g.6697401T>G , CM000681.1:g.6697401T>G	GRCh37
NC_000019.8:g.6648401T>G	NCBI36
NG_009557.1:g.28262A>C , LRG_27:g.28262A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1098A>C
ENST00000695652.1:c.2627A>C	ENSP00000512083.1:p.Tyr876Ser
ENST00000695653.1:c.659A>C	ENSP00000512084.1:p.Tyr220Ser
ENST00000695654.1:c.1874A>C	ENSP00000512085.1:p.Tyr625Ser
ENST00000695655.1:c.1691A>C	ENSP00000512086.1:n.1691A>C
ENST00000695692.1:n.2114A>C
ENST00000245907.11:c.2750A>C MANE Select	ENSP00000245907.4:p.Tyr917Ser
ENST00000245907.10:c.2750A>C	ENSP00000245907.4:p.Tyr917Ser
ENST00000594005.1:n.326A>C
NM_000064.3:c.2750A>C	NP_000055.2:p.Tyr917Ser
NM_000064.4:c.2750A>C MANE Select	NP_000055.2:p.Tyr917Ser