Canonical Allele Identifier: CA2320551550
Gene: C3 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000695651.1:n.2648C=
ENST00000695653.1:c.2209C= ENSP00000512084.1:p.Leu737=
ENST00000695654.1:c.3325C= ENSP00000512085.1:p.Leu1109=
ENST00000695689.1:c.271C= ENSP00000512101.1:n.271C=
ENST00000695690.1:n.491C=
ENST00000695691.1:n.491C=
ENST00000245907.11:c.4300C= MANE Select ENSP00000245907.4:p.Leu1434=
ENST00000245907.10:c.4300C= ENSP00000245907.4:p.Leu1434=
ENST00000596548.1:c.421C= ENSP00000469744.1:p.Leu141=
ENST00000599899.5:n.1259C=
ENST00000601008.1:c.242-4033C= ENSP00000471384.1:n.242-4033C=
NM_000064.3:c.4300C= NP_000055.2:p.Leu1434=
NM_000064.4:c.4300C= MANE Select NP_000055.2:p.Leu1434=