Canonical Allele Identifier: CA403618208

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6685006G>T (hg19) ; chr19:g.6684995G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6684995G>T , CM000681.2:g.6684995G>T	GRCh38
NC_000019.9:g.6685006G>T , CM000681.1:g.6685006G>T	GRCh37
NC_000019.8:g.6636006G>T	NCBI36
NG_009557.1:g.40657C>A , LRG_27:g.40657C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2310C>A
ENST00000695653.1:c.1871C>A	ENSP00000512084.1:p.Ser624Ter
ENST00000695654.1:c.2987C>A	ENSP00000512085.1:p.Ser996Ter
ENST00000695690.1:n.153C>A
ENST00000695691.1:n.153C>A
ENST00000245907.11:c.3962C>A MANE Select	ENSP00000245907.4:p.Ser1321Ter
ENST00000245907.10:c.3962C>A	ENSP00000245907.4:p.Ser1321Ter
ENST00000596238.1:n.405C>A
ENST00000596548.1:c.44C>A	ENSP00000469744.1:p.Ser15Ter
ENST00000601008.1:c.241+1751C>A	ENSP00000471384.1:n.241+1751C>A
NM_000064.3:c.3962C>A	NP_000055.2:p.Ser1321Ter
NM_000064.4:c.3962C>A MANE Select	NP_000055.2:p.Ser1321Ter