Canonical Allele Identifier: CA403632869

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697437G>A (hg19) ; chr19:g.6697426G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697426G>A , CM000681.2:g.6697426G>A	GRCh38
NC_000019.9:g.6697437G>A , CM000681.1:g.6697437G>A	GRCh37
NC_000019.8:g.6648437G>A	NCBI36
NG_009557.1:g.28226C>T , LRG_27:g.28226C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1062C>T
ENST00000695652.1:c.2591C>T	ENSP00000512083.1:p.Thr864Ile
ENST00000695653.1:c.623C>T	ENSP00000512084.1:p.Thr208Ile
ENST00000695654.1:c.1838C>T	ENSP00000512085.1:p.Thr613Ile
ENST00000695655.1:c.1655C>T	ENSP00000512086.1:n.1655C>T
ENST00000695692.1:n.2078C>T
ENST00000245907.11:c.2714C>T MANE Select	ENSP00000245907.4:p.Thr905Ile
ENST00000245907.10:c.2714C>T	ENSP00000245907.4:p.Thr905Ile
ENST00000594005.1:n.290C>T
NM_000064.3:c.2714C>T	NP_000055.2:p.Thr905Ile
NM_000064.4:c.2714C>T MANE Select	NP_000055.2:p.Thr905Ile