Canonical Allele Identifier: CA505192465

Gene: C3

Linked Data

• gnomAD v4: 19-6697685-A-G
• MyVariant Identifiers: chr19:g.6697696A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697685A>G , CM000681.2:g.6697685A>G	GRCh38
NC_000019.9:g.6697696A>G , CM000681.1:g.6697696A>G	GRCh37
NC_000019.8:g.6648696A>G	NCBI36
NG_009557.1:g.27967T>C , LRG_27:g.27967T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.898T>C
ENST00000695652.1:c.2427T>C	ENSP00000512083.1:p.Val809=
ENST00000695653.1:c.459T>C	ENSP00000512084.1:p.Val153=
ENST00000695654.1:c.1674T>C	ENSP00000512085.1:p.Val558=
ENST00000695655.1:c.1491T>C	ENSP00000512086.1:n.1491T>C
ENST00000695692.1:n.1914T>C
ENST00000245907.11:c.2550T>C MANE Select	ENSP00000245907.4:p.Val850=
ENST00000245907.10:c.2550T>C	ENSP00000245907.4:p.Val850=
ENST00000594005.1:n.31T>C
ENST00000602053.1:n.598T>C
NM_000064.3:c.2550T>C	NP_000055.2:p.Val850=
NM_000064.4:c.2550T>C MANE Select	NP_000055.2:p.Val850=