Canonical Allele Identifier: CA403633891

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697707T>A (hg19) ; chr19:g.6697696T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697696T>A , CM000681.2:g.6697696T>A	GRCh38
NC_000019.9:g.6697707T>A , CM000681.1:g.6697707T>A	GRCh37
NC_000019.8:g.6648707T>A	NCBI36
NG_009557.1:g.27956A>T , LRG_27:g.27956A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.887A>T
ENST00000695652.1:c.2416A>T	ENSP00000512083.1:p.Ile806Phe
ENST00000695653.1:c.448A>T	ENSP00000512084.1:p.Ile150Phe
ENST00000695654.1:c.1663A>T	ENSP00000512085.1:p.Ile555Phe
ENST00000695655.1:c.1480A>T	ENSP00000512086.1:n.1480A>T
ENST00000695692.1:n.1903A>T
ENST00000245907.11:c.2539A>T MANE Select	ENSP00000245907.4:p.Ile847Phe
ENST00000245907.10:c.2539A>T	ENSP00000245907.4:p.Ile847Phe
ENST00000594005.1:n.20A>T
ENST00000602053.1:n.587A>T
NM_000064.3:c.2539A>T	NP_000055.2:p.Ile847Phe
NM_000064.4:c.2539A>T MANE Select	NP_000055.2:p.Ile847Phe