Canonical Allele Identifier: CA403632724

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697402A>G (hg19) ; chr19:g.6697391A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697391A>G , CM000681.2:g.6697391A>G	GRCh38
NC_000019.9:g.6697402A>G , CM000681.1:g.6697402A>G	GRCh37
NC_000019.8:g.6648402A>G	NCBI36
NG_009557.1:g.28261T>C , LRG_27:g.28261T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1097T>C
ENST00000695652.1:c.2626T>C	ENSP00000512083.1:p.Tyr876His
ENST00000695653.1:c.658T>C	ENSP00000512084.1:p.Tyr220His
ENST00000695654.1:c.1873T>C	ENSP00000512085.1:p.Tyr625His
ENST00000695655.1:c.1690T>C	ENSP00000512086.1:n.1690T>C
ENST00000695692.1:n.2113T>C
ENST00000245907.11:c.2749T>C MANE Select	ENSP00000245907.4:p.Tyr917His
ENST00000245907.10:c.2749T>C	ENSP00000245907.4:p.Tyr917His
ENST00000594005.1:n.325T>C
NM_000064.3:c.2749T>C	NP_000055.2:p.Tyr917His
NM_000064.4:c.2749T>C MANE Select	NP_000055.2:p.Tyr917His