Canonical Allele Identifier: CA403612852

Gene: C3

Linked Data

• gnomAD v4: 19-6679482-G-C
• MyVariant Identifiers: chr19:g.6679493G>C (hg19) ; chr19:g.6679482G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679482G>C , CM000681.2:g.6679482G>C	GRCh38
NC_000019.9:g.6679493G>C , CM000681.1:g.6679493G>C	GRCh37
NC_000019.8:g.6630493G>C	NCBI36
NG_009557.1:g.46170C>G , LRG_27:g.46170C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2819C>G
ENST00000695653.1:c.2380C>G	ENSP00000512084.1:p.Arg794Gly
ENST00000695654.1:c.3496C>G	ENSP00000512085.1:p.Arg1166Gly
ENST00000695689.1:c.442C>G	ENSP00000512101.1:n.442C>G
ENST00000695690.1:n.1536C>G
ENST00000695691.1:n.1332C>G
ENST00000245907.11:c.4471C>G MANE Select	ENSP00000245907.4:p.Arg1491Gly
ENST00000245907.10:c.4471C>G	ENSP00000245907.4:p.Arg1491Gly
ENST00000599668.1:n.66C>G
ENST00000599899.5:n.1430C>G
ENST00000601008.1:c.242-1524C>G	ENSP00000471384.1:n.242-1524C>G
NM_000064.3:c.4471C>G	NP_000055.2:p.Arg1491Gly
NM_000064.4:c.4471C>G MANE Select	NP_000055.2:p.Arg1491Gly