Canonical Allele Identifier: CA403612774

Gene: C3

Linked Data

• dbSNP Id: rs1917802152
• MyVariant Identifiers: chr19:g.6679460G>T (hg19) ; chr19:g.6679449G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679449G>T , CM000681.2:g.6679449G>T	GRCh38
NC_000019.9:g.6679460G>T , CM000681.1:g.6679460G>T	GRCh37
NC_000019.8:g.6630460G>T	NCBI36
NG_009557.1:g.46203C>A , LRG_27:g.46203C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2852C>A
ENST00000695653.1:c.2413C>A	ENSP00000512084.1:p.Leu805Met
ENST00000695654.1:c.3529C>A	ENSP00000512085.1:p.Leu1177Met
ENST00000695689.1:c.475C>A	ENSP00000512101.1:n.475C>A
ENST00000695690.1:n.1569C>A
ENST00000695691.1:n.1365C>A
ENST00000245907.11:c.4504C>A MANE Select	ENSP00000245907.4:p.Leu1502Met
ENST00000245907.10:c.4504C>A	ENSP00000245907.4:p.Leu1502Met
ENST00000599668.1:n.99C>A
ENST00000599899.5:n.1463C>A
ENST00000601008.1:c.242-1491C>A	ENSP00000471384.1:n.242-1491C>A
NM_000064.3:c.4504C>A	NP_000055.2:p.Leu1502Met
NM_000064.4:c.4504C>A MANE Select	NP_000055.2:p.Leu1502Met