Canonical Allele Identifier: CA403633037

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697480T>G (hg19) ; chr19:g.6697469T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697469T>G , CM000681.2:g.6697469T>G	GRCh38
NC_000019.9:g.6697480T>G , CM000681.1:g.6697480T>G	GRCh37
NC_000019.8:g.6648480T>G	NCBI36
NG_009557.1:g.28183A>C , LRG_27:g.28183A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1019A>C
ENST00000695652.1:c.2548A>C	ENSP00000512083.1:p.Lys850Gln
ENST00000695653.1:c.580A>C	ENSP00000512084.1:p.Lys194Gln
ENST00000695654.1:c.1795A>C	ENSP00000512085.1:p.Lys599Gln
ENST00000695655.1:c.1612A>C	ENSP00000512086.1:n.1612A>C
ENST00000695692.1:n.2035A>C
ENST00000245907.11:c.2671A>C MANE Select	ENSP00000245907.4:p.Lys891Gln
ENST00000245907.10:c.2671A>C	ENSP00000245907.4:p.Lys891Gln
ENST00000594005.1:n.247A>C
NM_000064.3:c.2671A>C	NP_000055.2:p.Lys891Gln
NM_000064.4:c.2671A>C MANE Select	NP_000055.2:p.Lys891Gln