Canonical Allele Identifier: CA884129601

Gene: C3

Linked Data

• dbSNP Id: rs759927155
• MyVariant Identifiers: chr19:g.6682047G>C (hg19) ; chr19:g.6682036G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6682036G>C , CM000681.2:g.6682036G>C	GRCh38
NC_000019.9:g.6682047G>C , CM000681.1:g.6682047G>C	GRCh37
NC_000019.8:g.6633047G>C	NCBI36
NG_009557.1:g.43616C>G , LRG_27:g.43616C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2609-6C>G
ENST00000695653.1:c.2170-6C>G	ENSP00000512084.1:n.2170-6C>G
ENST00000695654.1:c.3286-6C>G	ENSP00000512085.1:n.3286-6C>G
ENST00000695689.1:c.232-6C>G	ENSP00000512101.1:n.232-6C>G
ENST00000695690.1:n.452-6C>G
ENST00000695691.1:n.452-6C>G
ENST00000245907.11:c.4261-6C>G MANE Select	ENSP00000245907.4:n.4261-6C>G
ENST00000245907.10:c.4261-6C>G	ENSP00000245907.4:n.4261-6C>G
ENST00000596548.1:c.382-6C>G	ENSP00000469744.1:n.382-6C>G
ENST00000599899.5:n.1220-6C>G
ENST00000601008.1:c.242-4078C>G	ENSP00000471384.1:n.242-4078C>G
NM_000064.3:c.4261-6C>G	NP_000055.2:n.4261-6C>G
NM_000064.4:c.4261-6C>G MANE Select	NP_000055.2:n.4261-6C>G