Canonical Allele Identifier: CA2320553367
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6686009C= , CM000681.2:g.6686009C= GRCh38
NC_000019.9:g.6686020C= , CM000681.1:g.6686020C= GRCh37
NC_000019.8:g.6637020C= NCBI36
NG_009557.1:g.39643G= , LRG_27:g.39643G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695651.1:n.2158+115G=
ENST00000695653.1:c.1719+115G= ENSP00000512084.1:n.1719+115G=
ENST00000695654.1:c.2835+115G= ENSP00000512085.1:n.2835+115G=
ENST00000245907.11:c.3810+115G= MANE Select ENSP00000245907.4:n.3810+115G=
ENST00000245907.10:c.3810+115G= ENSP00000245907.4:n.3810+115G=
ENST00000596238.1:n.253+115G=
ENST00000601008.1:c.241+737G= ENSP00000471384.1:n.241+737G=
NM_000064.3:c.3810+115G= NP_000055.2:n.3810+115G=
NM_000064.4:c.3810+115G= MANE Select NP_000055.2:n.3810+115G=