Canonical Allele Identifier: CA884148627

Gene: C3

Linked Data

• dbSNP Id: rs144643540
• gnomAD v3: 19-6709864-C-G
• gnomAD v4: 19-6709864-C-G
• MyVariant Identifiers: chr19:g.6709875C>G (hg19) ; chr19:g.6709864C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709864C>G , CM000681.2:g.6709864C>G	GRCh38
NC_000019.9:g.6709875C>G , CM000681.1:g.6709875C>G	GRCh37
NC_000019.8:g.6660875C>G	NCBI36
NG_009557.1:g.15788G>C , LRG_27:g.15788G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-22G>C	ENSP00000512083.1:n.1564-22G>C
ENST00000695654.1:c.811-22G>C	ENSP00000512085.1:n.811-22G>C
ENST00000695655.1:c.606G>C	ENSP00000512086.1:n.606G>C
ENST00000695692.1:n.1051-22G>C
ENST00000245907.11:c.1687-22G>C MANE Select	ENSP00000245907.4:n.1687-22G>C
ENST00000245907.10:c.1687-22G>C	ENSP00000245907.4:n.1687-22G>C
ENST00000600763.1:n.320-22G>C
NM_000064.3:c.1687-22G>C	NP_000055.2:n.1687-22G>C
NM_000064.4:c.1687-22G>C MANE Select	NP_000055.2:n.1687-22G>C