Canonical Allele Identifier: CA304798119

Gene: C3

Linked Data

• dbSNP Id: rs2230200
• gnomAD v4: 19-6713500-G-T
• MyVariant Identifiers: chr19:g.6713511G>T (hg19) ; chr19:g.6713500G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713500G>T , CM000681.2:g.6713500G>T	GRCh38
NC_000019.9:g.6713511G>T , CM000681.1:g.6713511G>T	GRCh37
NC_000019.8:g.6664511G>T	NCBI36
NG_009557.1:g.12152C>A , LRG_27:g.12152C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.660C>A	ENSP00000512083.1:p.Tyr220Ter
ENST00000695692.1:n.107C>A
ENST00000245907.11:c.783C>A MANE Select	ENSP00000245907.4:p.Tyr261Ter
ENST00000245907.10:c.783C>A	ENSP00000245907.4:p.Tyr261Ter
ENST00000595577.1:n.287C>A
ENST00000597442.5:n.33C>A
NM_000064.3:c.783C>A	NP_000055.2:p.Tyr261Ter
NM_000064.4:c.783C>A MANE Select	NP_000055.2:p.Tyr261Ter