Canonical Allele Identifier: CA304794703

Gene: C3

Linked Data

• dbSNP Id: rs965096873
• gnomAD v4: 19-6709965-G-T
• MyVariant Identifiers: chr19:g.6709976G>T (hg19) ; chr19:g.6709965G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709965G>T , CM000681.2:g.6709965G>T	GRCh38
NC_000019.9:g.6709976G>T , CM000681.1:g.6709976G>T	GRCh37
NC_000019.8:g.6660976G>T	NCBI36
NG_009557.1:g.15687C>A , LRG_27:g.15687C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-123C>A	ENSP00000512083.1:n.1564-123C>A
ENST00000695654.1:c.811-123C>A	ENSP00000512085.1:n.811-123C>A
ENST00000695655.1:c.592-87C>A	ENSP00000512086.1:n.592-87C>A
ENST00000695692.1:n.1051-123C>A
ENST00000245907.11:c.1687-123C>A MANE Select	ENSP00000245907.4:n.1687-123C>A
ENST00000245907.10:c.1687-123C>A	ENSP00000245907.4:n.1687-123C>A
ENST00000600763.1:n.320-123C>A
NM_000064.3:c.1687-123C>A	NP_000055.2:n.1687-123C>A
NM_000064.4:c.1687-123C>A MANE Select	NP_000055.2:n.1687-123C>A