Canonical Allele Identifier: CA505123978

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6690682G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6690671G>T , CM000681.2:g.6690671G>T	GRCh38
NC_000019.9:g.6690682G>T , CM000681.1:g.6690682G>T	GRCh37
NC_000019.8:g.6641682G>T	NCBI36
NG_009557.1:g.34981C>A , LRG_27:g.34981C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000695651.1:n.1795C>A
ENST00000695652.1:c.3324C>A	ENSP00000512083.1:p.Ile1108=
ENST00000695653.1:c.1356C>A	ENSP00000512084.1:p.Ile452=
ENST00000695654.1:c.2514+2253C>A	ENSP00000512085.1:n.2514+2253C>A
ENST00000695655.1:c.2388C>A	ENSP00000512086.1:n.2388C>A
ENST00000695692.1:n.2811C>A
ENST00000245907.11:c.3447C>A MANE Select	ENSP00000245907.4:p.Ile1149=
ENST00000245907.10:c.3447C>A	ENSP00000245907.4:p.Ile1149=
ENST00000598805.2:n.217C>A
ENST00000601008.1:c.42C>A	ENSP00000471384.1:p.Ile14=
NM_000064.3:c.3447C>A	NP_000055.2:p.Ile1149=
NM_000064.4:c.3447C>A MANE Select	NP_000055.2:p.Ile1149=