Canonical Allele Identifier: CA403642585

Gene: C3

Linked Data

• gnomAD v4: 19-6713450-C-T
• MyVariant Identifiers: chr19:g.6713461C>T (hg19) ; chr19:g.6713450C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713450C>T , CM000681.2:g.6713450C>T	GRCh38
NC_000019.9:g.6713461C>T , CM000681.1:g.6713461C>T	GRCh37
NC_000019.8:g.6664461C>T	NCBI36
NG_009557.1:g.12202G>A , LRG_27:g.12202G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.710G>A	ENSP00000512083.1:p.Gly237Asp
ENST00000695692.1:n.157G>A
ENST00000245907.11:c.833G>A MANE Select	ENSP00000245907.4:p.Gly278Asp
ENST00000245907.10:c.833G>A	ENSP00000245907.4:p.Gly278Asp
ENST00000595577.1:n.337G>A
ENST00000597442.5:n.83G>A
NM_000064.3:c.833G>A	NP_000055.2:p.Gly278Asp
NM_000064.4:c.833G>A MANE Select	NP_000055.2:p.Gly278Asp