Canonical Allele Identifier: CA403642342

Gene: C3

Linked Data

• gnomAD v4: 19-6713306-C-T
• MyVariant Identifiers: chr19:g.6713317C>T (hg19) ; chr19:g.6713306C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713306C>T , CM000681.2:g.6713306C>T	GRCh38
NC_000019.9:g.6713317C>T , CM000681.1:g.6713317C>T	GRCh37
NC_000019.8:g.6664317C>T	NCBI36
NG_009557.1:g.12346G>A , LRG_27:g.12346G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.763G>A	ENSP00000512083.1:p.Gly255Ser
ENST00000695654.1:c.10G>A	ENSP00000512085.1:p.Gly4Ser
ENST00000695692.1:n.210G>A
ENST00000245907.11:c.886G>A MANE Select	ENSP00000245907.4:p.Gly296Ser
ENST00000245907.10:c.886G>A	ENSP00000245907.4:p.Gly296Ser
ENST00000594270.5:n.10G>A
ENST00000595577.1:n.390G>A
ENST00000597442.5:n.136G>A
NM_000064.3:c.886G>A	NP_000055.2:p.Gly296Ser
NM_000064.4:c.886G>A MANE Select	NP_000055.2:p.Gly296Ser