Canonical Allele Identifier: CA403632517

Gene: C3

Linked Data

• dbSNP Id: rs1967561397
• MyVariant Identifiers: chr19:g.6697368G>T (hg19) ; chr19:g.6697357G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697357G>T , CM000681.2:g.6697357G>T	GRCh38
NC_000019.9:g.6697368G>T , CM000681.1:g.6697368G>T	GRCh37
NC_000019.8:g.6648368G>T	NCBI36
NG_009557.1:g.28295C>A , LRG_27:g.28295C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1131C>A
ENST00000695652.1:c.2660C>A	ENSP00000512083.1:p.Ser887Tyr
ENST00000695653.1:c.692C>A	ENSP00000512084.1:p.Ser231Tyr
ENST00000695654.1:c.1907C>A	ENSP00000512085.1:p.Ser636Tyr
ENST00000695655.1:c.1724C>A	ENSP00000512086.1:n.1724C>A
ENST00000695692.1:n.2147C>A
ENST00000245907.11:c.2783C>A MANE Select	ENSP00000245907.4:p.Ser928Tyr
ENST00000245907.10:c.2783C>A	ENSP00000245907.4:p.Ser928Tyr
ENST00000594005.1:n.359C>A
NM_000064.3:c.2783C>A	NP_000055.2:p.Ser928Tyr
NM_000064.4:c.2783C>A MANE Select	NP_000055.2:p.Ser928Tyr