Canonical Allele Identifier: CA884138158

Gene: C3

Linked Data

• dbSNP Id: rs1200796294
• gnomAD v3: 19-6694916-A-G
• gnomAD v4: 19-6694916-A-G
• MyVariant Identifiers: chr19:g.6694927A>G (hg19) ; chr19:g.6694916A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6694916A>G , CM000681.2:g.6694916A>G	GRCh38
NC_000019.9:g.6694927A>G , CM000681.1:g.6694927A>G	GRCh37
NC_000019.8:g.6645927A>G	NCBI36
NG_009557.1:g.30736T>C , LRG_27:g.30736T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1299-282T>C
ENST00000695652.1:c.2828-282T>C	ENSP00000512083.1:n.2828-282T>C
ENST00000695653.1:c.860-282T>C	ENSP00000512084.1:n.860-282T>C
ENST00000695654.1:c.2075-282T>C	ENSP00000512085.1:n.2075-282T>C
ENST00000695655.1:c.1892-282T>C	ENSP00000512086.1:n.1892-282T>C
ENST00000695692.1:n.2315-282T>C
ENST00000245907.11:c.2951-282T>C MANE Select	ENSP00000245907.4:n.2951-282T>C
ENST00000245907.10:c.2951-282T>C	ENSP00000245907.4:n.2951-282T>C
NM_000064.3:c.2951-282T>C	NP_000055.2:n.2951-282T>C
NM_000064.4:c.2951-282T>C MANE Select	NP_000055.2:n.2951-282T>C