Canonical Allele Identifier: CA304794695

Gene: C3

Linked Data

• dbSNP Id: rs1018012112
• MyVariant Identifiers: chr19:g.6709952G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709952G>C , CM000681.2:g.6709952G>C	GRCh38
NC_000019.9:g.6709963G>C , CM000681.1:g.6709963G>C	GRCh37
NC_000019.8:g.6660963G>C	NCBI36
NG_009557.1:g.15700C>G , LRG_27:g.15700C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-110C>G	ENSP00000512083.1:n.1564-110C>G
ENST00000695654.1:c.811-110C>G	ENSP00000512085.1:n.811-110C>G
ENST00000695655.1:c.592-74C>G	ENSP00000512086.1:n.592-74C>G
ENST00000695692.1:n.1051-110C>G
ENST00000245907.11:c.1687-110C>G MANE Select	ENSP00000245907.4:n.1687-110C>G
ENST00000245907.10:c.1687-110C>G	ENSP00000245907.4:n.1687-110C>G
ENST00000600763.1:n.320-110C>G
NM_000064.3:c.1687-110C>G	NP_000055.2:n.1687-110C>G
NM_000064.4:c.1687-110C>G MANE Select	NP_000055.2:n.1687-110C>G