Canonical Allele Identifier: CA884140011

Gene: C3

Linked Data

• dbSNP Id: rs1244995257
• gnomAD v4: 19-6697291-G-C
• MyVariant Identifiers: chr19:g.6697302G>C (hg19) ; chr19:g.6697291G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697291G>C , CM000681.2:g.6697291G>C	GRCh38
NC_000019.9:g.6697302G>C , CM000681.1:g.6697302G>C	GRCh37
NC_000019.8:g.6648302G>C	NCBI36
NG_009557.1:g.28361C>G , LRG_27:g.28361C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1144+53C>G
ENST00000695652.1:c.2673+53C>G	ENSP00000512083.1:n.2673+53C>G
ENST00000695653.1:c.705+53C>G	ENSP00000512084.1:n.705+53C>G
ENST00000695654.1:c.1920+53C>G	ENSP00000512085.1:n.1920+53C>G
ENST00000695655.1:c.1737+53C>G	ENSP00000512086.1:n.1737+53C>G
ENST00000695692.1:n.2160+53C>G
ENST00000245907.11:c.2796+53C>G MANE Select	ENSP00000245907.4:n.2796+53C>G
ENST00000245907.10:c.2796+53C>G	ENSP00000245907.4:n.2796+53C>G
ENST00000594005.1:n.372+53C>G
NM_000064.3:c.2796+53C>G	NP_000055.2:n.2796+53C>G
NM_000064.4:c.2796+53C>G MANE Select	NP_000055.2:n.2796+53C>G