Canonical Allele Identifier: CA505192323

Gene: C3

Linked Data

• gnomAD v4: 19-6697461-C-G
• MyVariant Identifiers: chr19:g.6697472C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697461C>G , CM000681.2:g.6697461C>G	GRCh38
NC_000019.9:g.6697472C>G , CM000681.1:g.6697472C>G	GRCh37
NC_000019.8:g.6648472C>G	NCBI36
NG_009557.1:g.28191G>C , LRG_27:g.28191G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1027G>C
ENST00000695652.1:c.2556G>C	ENSP00000512083.1:p.Ser852=
ENST00000695653.1:c.588G>C	ENSP00000512084.1:p.Ser196=
ENST00000695654.1:c.1803G>C	ENSP00000512085.1:p.Ser601=
ENST00000695655.1:c.1620G>C	ENSP00000512086.1:n.1620G>C
ENST00000695692.1:n.2043G>C
ENST00000245907.11:c.2679G>C MANE Select	ENSP00000245907.4:p.Ser893=
ENST00000245907.10:c.2679G>C	ENSP00000245907.4:p.Ser893=
ENST00000594005.1:n.255G>C
NM_000064.3:c.2679G>C	NP_000055.2:p.Ser893=
NM_000064.4:c.2679G>C MANE Select	NP_000055.2:p.Ser893=