Canonical Allele Identifier: CA505192242

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697385A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697374A>G , CM000681.2:g.6697374A>G	GRCh38
NC_000019.9:g.6697385A>G , CM000681.1:g.6697385A>G	GRCh37
NC_000019.8:g.6648385A>G	NCBI36
NG_009557.1:g.28278T>C , LRG_27:g.28278T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1114T>C
ENST00000695652.1:c.2643T>C	ENSP00000512083.1:p.Ser881=
ENST00000695653.1:c.675T>C	ENSP00000512084.1:p.Ser225=
ENST00000695654.1:c.1890T>C	ENSP00000512085.1:p.Ser630=
ENST00000695655.1:c.1707T>C	ENSP00000512086.1:n.1707T>C
ENST00000695692.1:n.2130T>C
ENST00000245907.11:c.2766T>C MANE Select	ENSP00000245907.4:p.Ser922=
ENST00000245907.10:c.2766T>C	ENSP00000245907.4:p.Ser922=
ENST00000594005.1:n.342T>C
NM_000064.3:c.2766T>C	NP_000055.2:p.Ser922=
NM_000064.4:c.2766T>C MANE Select	NP_000055.2:p.Ser922=