Canonical Allele Identifier: CA403632871

Gene: C3

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1062C>G
ENST00000695652.1:c.2591C>G	ENSP00000512083.1:p.Thr864Ser
ENST00000695653.1:c.623C>G	ENSP00000512084.1:p.Thr208Ser
ENST00000695654.1:c.1838C>G	ENSP00000512085.1:p.Thr613Ser
ENST00000695655.1:c.1655C>G	ENSP00000512086.1:n.1655C>G
ENST00000695692.1:n.2078C>G
ENST00000245907.11:c.2714C>G MANE Select	ENSP00000245907.4:p.Thr905Ser
ENST00000245907.10:c.2714C>G	ENSP00000245907.4:p.Thr905Ser
ENST00000594005.1:n.290C>G
NM_000064.3:c.2714C>G	NP_000055.2:p.Thr905Ser
NM_000064.4:c.2714C>G MANE Select	NP_000055.2:p.Thr905Ser