Canonical Allele Identifier: CA403633434

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697540C>G (hg19) ; chr19:g.6697529C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697529C>G , CM000681.2:g.6697529C>G	GRCh38
NC_000019.9:g.6697540C>G , CM000681.1:g.6697540C>G	GRCh37
NC_000019.8:g.6648540C>G	NCBI36
NG_009557.1:g.28123G>C , LRG_27:g.28123G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.959G>C
ENST00000695652.1:c.2488G>C	ENSP00000512083.1:p.Ala830Pro
ENST00000695653.1:c.520G>C	ENSP00000512084.1:p.Ala174Pro
ENST00000695654.1:c.1735G>C	ENSP00000512085.1:p.Ala579Pro
ENST00000695655.1:c.1552G>C	ENSP00000512086.1:n.1552G>C
ENST00000695692.1:n.1975G>C
ENST00000245907.11:c.2611G>C MANE Select	ENSP00000245907.4:p.Ala871Pro
ENST00000245907.10:c.2611G>C	ENSP00000245907.4:p.Ala871Pro
ENST00000594005.1:n.187G>C
NM_000064.3:c.2611G>C	NP_000055.2:p.Ala871Pro
NM_000064.4:c.2611G>C MANE Select	NP_000055.2:p.Ala871Pro