Canonical Allele Identifier: CA304794710

Gene: C3

Linked Data

• dbSNP Id: rs1027997642
• gnomAD v4: 19-6709982-A-G
• MyVariant Identifiers: chr19:g.6709993A>G (hg19) ; chr19:g.6709982A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709982A>G , CM000681.2:g.6709982A>G	GRCh38
NC_000019.9:g.6709993A>G , CM000681.1:g.6709993A>G	GRCh37
NC_000019.8:g.6660993A>G	NCBI36
NG_009557.1:g.15670T>C , LRG_27:g.15670T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-140T>C	ENSP00000512083.1:n.1564-140T>C
ENST00000695654.1:c.811-140T>C	ENSP00000512085.1:n.811-140T>C
ENST00000695655.1:c.592-104T>C	ENSP00000512086.1:n.592-104T>C
ENST00000695692.1:n.1051-140T>C
ENST00000245907.11:c.1687-140T>C MANE Select	ENSP00000245907.4:n.1687-140T>C
ENST00000245907.10:c.1687-140T>C	ENSP00000245907.4:n.1687-140T>C
ENST00000600763.1:n.320-140T>C
NM_000064.3:c.1687-140T>C	NP_000055.2:n.1687-140T>C
NM_000064.4:c.1687-140T>C MANE Select	NP_000055.2:n.1687-140T>C