Canonical Allele Identifier: CA403618658

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6685147A>T (hg19) ; chr19:g.6685136A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6685136A>T , CM000681.2:g.6685136A>T	GRCh38
NC_000019.9:g.6685147A>T , CM000681.1:g.6685147A>T	GRCh37
NC_000019.8:g.6636147A>T	NCBI36
NG_009557.1:g.40516T>A , LRG_27:g.40516T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2169T>A
ENST00000695653.1:c.1730T>A	ENSP00000512084.1:p.Met577Lys
ENST00000695654.1:c.2846T>A	ENSP00000512085.1:p.Met949Lys
ENST00000695690.1:n.12T>A
ENST00000695691.1:n.12T>A
ENST00000245907.11:c.3821T>A MANE Select	ENSP00000245907.4:p.Met1274Lys
ENST00000245907.10:c.3821T>A	ENSP00000245907.4:p.Met1274Lys
ENST00000596238.1:n.264T>A
ENST00000601008.1:c.241+1610T>A	ENSP00000471384.1:n.241+1610T>A
NM_000064.3:c.3821T>A	NP_000055.2:p.Met1274Lys
NM_000064.4:c.3821T>A MANE Select	NP_000055.2:p.Met1274Lys