Canonical Allele Identifier: CA2813446783

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6714287A>C , CM000681.2:g.6714287A>C	GRCh38
NC_000019.9:g.6714298A>C , CM000681.1:g.6714298A>C	GRCh37
NC_000019.8:g.6665298A>C	NCBI36
NG_009557.1:g.11365T>G , LRG_27:g.11365T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.477-39T>G	ENSP00000512083.1:n.477-39T>G
ENST00000245907.11:c.600-39T>G MANE Select	ENSP00000245907.4:n.600-39T>G
ENST00000245907.10:c.600-39T>G	ENSP00000245907.4:n.600-39T>G
ENST00000595577.1:n.65T>G
NM_000064.3:c.600-39T>G	NP_000055.2:n.600-39T>G
NM_000064.4:c.600-39T>G MANE Select	NP_000055.2:n.600-39T>G