Canonical Allele Identifier: CA2813446789

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6714292C>A , CM000681.2:g.6714292C>A	GRCh38
NC_000019.9:g.6714303C>A , CM000681.1:g.6714303C>A	GRCh37
NC_000019.8:g.6665303C>A	NCBI36
NG_009557.1:g.11360G>T , LRG_27:g.11360G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.477-44G>T	ENSP00000512083.1:n.477-44G>T
ENST00000245907.11:c.600-44G>T MANE Select	ENSP00000245907.4:n.600-44G>T
ENST00000245907.10:c.600-44G>T	ENSP00000245907.4:n.600-44G>T
ENST00000595577.1:n.60G>T
NM_000064.3:c.600-44G>T	NP_000055.2:n.600-44G>T
NM_000064.4:c.600-44G>T MANE Select	NP_000055.2:n.600-44G>T