Canonical Allele Identifier: CA884128496

Gene: C3

Linked Data

• dbSNP Id: rs1310751182
• gnomAD v4: 19-6679524-G-C
• MyVariant Identifiers: chr19:g.6679535G>C (hg19) ; chr19:g.6679524G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679524G>C , CM000681.2:g.6679524G>C	GRCh38
NC_000019.9:g.6679535G>C , CM000681.1:g.6679535G>C	GRCh37
NC_000019.8:g.6630535G>C	NCBI36
NG_009557.1:g.46128C>G , LRG_27:g.46128C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2805-28C>G
ENST00000695653.1:c.2366-28C>G	ENSP00000512084.1:n.2366-28C>G
ENST00000695654.1:c.3482-28C>G	ENSP00000512085.1:n.3482-28C>G
ENST00000695689.1:c.428-28C>G	ENSP00000512101.1:n.428-28C>G
ENST00000695690.1:n.1522-28C>G
ENST00000695691.1:n.1318-28C>G
ENST00000245907.11:c.4457-28C>G MANE Select	ENSP00000245907.4:n.4457-28C>G
ENST00000245907.10:c.4457-28C>G	ENSP00000245907.4:n.4457-28C>G
ENST00000599668.1:n.52-28C>G
ENST00000599899.5:n.1416-28C>G
ENST00000601008.1:c.242-1566C>G	ENSP00000471384.1:n.242-1566C>G
NM_000064.3:c.4457-28C>G	NP_000055.2:n.4457-28C>G
NM_000064.4:c.4457-28C>G MANE Select	NP_000055.2:n.4457-28C>G