Canonical Allele Identifier: CA9128986

Gene: C3

Linked Data

• dbSNP Id: rs769080198
• ExAC: 19:6697445 C / G
• gnomAD v2: 19-6697445-C-G
• gnomAD v3: 19-6697434-C-G
• gnomAD v4: 19-6697434-C-G
• MyVariant Identifiers: chr19:g.6697445C>G (hg19) ; chr19:g.6697434C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697434C>G , CM000681.2:g.6697434C>G	GRCh38
NC_000019.9:g.6697445C>G , CM000681.1:g.6697445C>G	GRCh37
NC_000019.8:g.6648445C>G	NCBI36
NG_009557.1:g.28218G>C , LRG_27:g.28218G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1054G>C
ENST00000695652.1:c.2583G>C	ENSP00000512083.1:p.Pro861=
ENST00000695653.1:c.615G>C	ENSP00000512084.1:p.Pro205=
ENST00000695654.1:c.1830G>C	ENSP00000512085.1:p.Pro610=
ENST00000695655.1:c.1647G>C	ENSP00000512086.1:n.1647G>C
ENST00000695692.1:n.2070G>C
ENST00000245907.11:c.2706G>C MANE Select	ENSP00000245907.4:p.Pro902=
ENST00000245907.10:c.2706G>C	ENSP00000245907.4:p.Pro902=
ENST00000594005.1:n.282G>C
NM_000064.3:c.2706G>C	NP_000055.2:p.Pro902=
NM_000064.4:c.2706G>C MANE Select	NP_000055.2:p.Pro902=