Canonical Allele Identifier: CA884140477

Gene: C3

Linked Data

• ClinVar Variation Id: 2881522
• ClinVar RCV Id: RCV003708117
• dbSNP Id: rs1329214450
• MyVariant Identifiers: chr19:g.6697576G>C (hg19) ; chr19:g.6697565G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697565G>C , CM000681.2:g.6697565G>C	GRCh38
NC_000019.9:g.6697576G>C , CM000681.1:g.6697576G>C	GRCh37
NC_000019.8:g.6648576G>C	NCBI36
NG_009557.1:g.28087C>G , LRG_27:g.28087C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.932-9C>G
ENST00000695652.1:c.2461-9C>G	ENSP00000512083.1:n.2461-9C>G
ENST00000695653.1:c.493-9C>G	ENSP00000512084.1:n.493-9C>G
ENST00000695654.1:c.1708-9C>G	ENSP00000512085.1:n.1708-9C>G
ENST00000695655.1:c.1525-9C>G	ENSP00000512086.1:n.1525-9C>G
ENST00000695692.1:n.1948-9C>G
ENST00000245907.11:c.2584-9C>G MANE Select	ENSP00000245907.4:n.2584-9C>G
ENST00000245907.10:c.2584-9C>G	ENSP00000245907.4:n.2584-9C>G
ENST00000594005.1:n.151C>G
NM_000064.3:c.2584-9C>G	NP_000055.2:n.2584-9C>G
NM_000064.4:c.2584-9C>G MANE Select	NP_000055.2:n.2584-9C>G