Canonical Allele Identifier: CA403614838

Gene: C3

Linked Data

• dbSNP Id: rs1599498134
• MyVariant Identifiers: chr19:g.6682002G>T (hg19) ; chr19:g.6681991G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6681991G>T , CM000681.2:g.6681991G>T	GRCh38
NC_000019.9:g.6682002G>T , CM000681.1:g.6682002G>T	GRCh37
NC_000019.8:g.6633002G>T	NCBI36
NG_009557.1:g.43661C>A , LRG_27:g.43661C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2648C>A
ENST00000695653.1:c.2209C>A	ENSP00000512084.1:p.Leu737Met
ENST00000695654.1:c.3325C>A	ENSP00000512085.1:p.Leu1109Met
ENST00000695689.1:c.271C>A	ENSP00000512101.1:n.271C>A
ENST00000695690.1:n.491C>A
ENST00000695691.1:n.491C>A
ENST00000245907.11:c.4300C>A MANE Select	ENSP00000245907.4:p.Leu1434Met
ENST00000245907.10:c.4300C>A	ENSP00000245907.4:p.Leu1434Met
ENST00000596548.1:c.421C>A	ENSP00000469744.1:p.Leu141Met
ENST00000599899.5:n.1259C>A
ENST00000601008.1:c.242-4033C>A	ENSP00000471384.1:n.242-4033C>A
NM_000064.3:c.4300C>A	NP_000055.2:p.Leu1434Met
NM_000064.4:c.4300C>A MANE Select	NP_000055.2:p.Leu1434Met