Canonical Allele Identifier: CA884132257

Gene: C3

Linked Data

• dbSNP Id: rs1459646835
• MyVariant Identifiers: chr19:g.6714157C>T (hg19) ; chr19:g.6714146C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6714146C>T , CM000681.2:g.6714146C>T	GRCh38
NC_000019.9:g.6714157C>T , CM000681.1:g.6714157C>T	GRCh37
NC_000019.8:g.6665157C>T	NCBI36
NG_009557.1:g.11506G>A , LRG_27:g.11506G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.559+20G>A	ENSP00000512083.1:n.559+20G>A
ENST00000245907.11:c.682+20G>A MANE Select	ENSP00000245907.4:n.682+20G>A
ENST00000245907.10:c.682+20G>A	ENSP00000245907.4:n.682+20G>A
ENST00000595577.1:n.186+20G>A
NM_000064.3:c.682+20G>A	NP_000055.2:n.682+20G>A
NM_000064.4:c.682+20G>A MANE Select	NP_000055.2:n.682+20G>A