Canonical Allele Identifier: CA403614863

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6682006A>C (hg19) ; chr19:g.6681995A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6681995A>C , CM000681.2:g.6681995A>C	GRCh38
NC_000019.9:g.6682006A>C , CM000681.1:g.6682006A>C	GRCh37
NC_000019.8:g.6633006A>C	NCBI36
NG_009557.1:g.43657T>G , LRG_27:g.43657T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2644T>G
ENST00000695653.1:c.2205T>G	ENSP00000512084.1:p.Tyr735Ter
ENST00000695654.1:c.3321T>G	ENSP00000512085.1:p.Tyr1107Ter
ENST00000695689.1:c.267T>G	ENSP00000512101.1:n.267T>G
ENST00000695690.1:n.487T>G
ENST00000695691.1:n.487T>G
ENST00000245907.11:c.4296T>G MANE Select	ENSP00000245907.4:p.Tyr1432Ter
ENST00000245907.10:c.4296T>G	ENSP00000245907.4:p.Tyr1432Ter
ENST00000596548.1:c.417T>G	ENSP00000469744.1:p.Tyr139Ter
ENST00000599899.5:n.1255T>G
ENST00000601008.1:c.242-4037T>G	ENSP00000471384.1:n.242-4037T>G
NM_000064.3:c.4296T>G	NP_000055.2:p.Tyr1432Ter
NM_000064.4:c.4296T>G MANE Select	NP_000055.2:p.Tyr1432Ter