Canonical Allele Identifier: CA505122407

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6682216A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6682205A>C , CM000681.2:g.6682205A>C	GRCh38
NC_000019.9:g.6682216A>C , CM000681.1:g.6682216A>C	GRCh37
NC_000019.8:g.6633216A>C	NCBI36
NG_009557.1:g.43447T>G , LRG_27:g.43447T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2545T>G
ENST00000695653.1:c.2106T>G	ENSP00000512084.1:p.Thr702=
ENST00000695654.1:c.3222T>G	ENSP00000512085.1:p.Thr1074=
ENST00000695689.1:c.168T>G	ENSP00000512101.1:n.168T>G
ENST00000695690.1:n.388T>G
ENST00000695691.1:n.388T>G
ENST00000245907.11:c.4197T>G MANE Select	ENSP00000245907.4:p.Thr1399=
ENST00000245907.10:c.4197T>G	ENSP00000245907.4:p.Thr1399=
ENST00000596548.1:c.318T>G	ENSP00000469744.1:p.Thr106=
ENST00000599899.5:n.1156T>G
ENST00000601008.1:c.242-4247T>G	ENSP00000471384.1:n.242-4247T>G
NM_000064.3:c.4197T>G	NP_000055.2:p.Thr1399=
NM_000064.4:c.4197T>G MANE Select	NP_000055.2:p.Thr1399=