Canonical Allele Identifier: CA403643086

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6714175A>G (hg19) ; chr19:g.6714164A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6714164A>G , CM000681.2:g.6714164A>G	GRCh38
NC_000019.9:g.6714175A>G , CM000681.1:g.6714175A>G	GRCh37
NC_000019.8:g.6665175A>G	NCBI36
NG_009557.1:g.11488T>C , LRG_27:g.11488T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.559+2T>C	ENSP00000512083.1:n.559+2T>C
ENST00000245907.11:c.682+2T>C MANE Select	ENSP00000245907.4:n.682+2T>C
ENST00000245907.10:c.682+2T>C	ENSP00000245907.4:n.682+2T>C
ENST00000595577.1:n.186+2T>C
NM_000064.3:c.682+2T>C	NP_000055.2:n.682+2T>C
NM_000064.4:c.682+2T>C MANE Select	NP_000055.2:n.682+2T>C