Canonical Allele Identifier: CA884138151

Gene: C3

Linked Data

• dbSNP Id: rs1453530685
• MyVariant Identifiers: chr19:g.6694902C>T (hg19) ; chr19:g.6694891C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6694891C>T , CM000681.2:g.6694891C>T	GRCh38
NC_000019.9:g.6694902C>T , CM000681.1:g.6694902C>T	GRCh37
NC_000019.8:g.6645902C>T	NCBI36
NG_009557.1:g.30761G>A , LRG_27:g.30761G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1299-257G>A
ENST00000695652.1:c.2828-257G>A	ENSP00000512083.1:n.2828-257G>A
ENST00000695653.1:c.860-257G>A	ENSP00000512084.1:n.860-257G>A
ENST00000695654.1:c.2075-257G>A	ENSP00000512085.1:n.2075-257G>A
ENST00000695655.1:c.1892-257G>A	ENSP00000512086.1:n.1892-257G>A
ENST00000695692.1:n.2315-257G>A
ENST00000245907.11:c.2951-257G>A MANE Select	ENSP00000245907.4:n.2951-257G>A
ENST00000245907.10:c.2951-257G>A	ENSP00000245907.4:n.2951-257G>A
NM_000064.3:c.2951-257G>A	NP_000055.2:n.2951-257G>A
NM_000064.4:c.2951-257G>A MANE Select	NP_000055.2:n.2951-257G>A