Canonical Allele Identifier: CA884138162

Gene: C3

Linked Data

• dbSNP Id: rs1213750809
• gnomAD v3: 19-6694926-T-A
• gnomAD v4: 19-6694926-T-A
• MyVariant Identifiers: chr19:g.6694937T>A (hg19) ; chr19:g.6694926T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6694926T>A , CM000681.2:g.6694926T>A	GRCh38
NC_000019.9:g.6694937T>A , CM000681.1:g.6694937T>A	GRCh37
NC_000019.8:g.6645937T>A	NCBI36
NG_009557.1:g.30726A>T , LRG_27:g.30726A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1299-292A>T
ENST00000695652.1:c.2828-292A>T	ENSP00000512083.1:n.2828-292A>T
ENST00000695653.1:c.860-292A>T	ENSP00000512084.1:n.860-292A>T
ENST00000695654.1:c.2075-292A>T	ENSP00000512085.1:n.2075-292A>T
ENST00000695655.1:c.1892-292A>T	ENSP00000512086.1:n.1892-292A>T
ENST00000695692.1:n.2315-292A>T
ENST00000245907.11:c.2951-292A>T MANE Select	ENSP00000245907.4:n.2951-292A>T
ENST00000245907.10:c.2951-292A>T	ENSP00000245907.4:n.2951-292A>T
NM_000064.3:c.2951-292A>T	NP_000055.2:n.2951-292A>T
NM_000064.4:c.2951-292A>T MANE Select	NP_000055.2:n.2951-292A>T