Canonical Allele Identifier: CA2320568060

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713666C= , CM000681.2:g.6713666C=	GRCh38
NC_000019.9:g.6713677C= , CM000681.1:g.6713677C=	GRCh37
NC_000019.8:g.6664677C=	NCBI36
NG_009557.1:g.11986G= , LRG_27:g.11986G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.651-157G=	ENSP00000512083.1:n.651-157G=
ENST00000245907.11:c.774-157G= MANE Select	ENSP00000245907.4:n.774-157G=
ENST00000245907.10:c.774-157G=	ENSP00000245907.4:n.774-157G=
ENST00000595577.1:n.278-157G=
ENST00000597442.5:n.23+100G=
NM_000064.3:c.774-157G=	NP_000055.2:n.774-157G=
NM_000064.4:c.774-157G= MANE Select	NP_000055.2:n.774-157G=