Canonical Allele Identifier: CA2320557825

Gene: C3

Linked Data

• dbSNP Id: rs10402876

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6694990G>A , CM000681.2:g.6694990G>A	GRCh38
NC_000019.9:g.6695001G>A , CM000681.1:g.6695001G>A	GRCh37
NC_000019.8:g.6646001G>A	NCBI36
NG_009557.1:g.30662C>T , LRG_27:g.30662C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000695651.1:n.1299-356C>T
ENST00000695652.1:c.2828-356C>T	ENSP00000512083.1:n.2828-356C>T
ENST00000695653.1:c.860-356C>T	ENSP00000512084.1:n.860-356C>T
ENST00000695654.1:c.2075-356C>T	ENSP00000512085.1:n.2075-356C>T
ENST00000695655.1:c.1892-356C>T	ENSP00000512086.1:n.1892-356C>T
ENST00000695692.1:n.2315-356C>T
ENST00000245907.11:c.2951-356C>T MANE Select	ENSP00000245907.4:n.2951-356C>T
ENST00000245907.10:c.2951-356C>T	ENSP00000245907.4:n.2951-356C>T
NM_000064.3:c.2951-356C>T	NP_000055.2:n.2951-356C>T
NM_000064.4:c.2951-356C>T MANE Select	NP_000055.2:n.2951-356C>T