Canonical Allele Identifier: CA403639140

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6709697T>A (hg19) ; chr19:g.6709686T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709686T>A , CM000681.2:g.6709686T>A	GRCh38
NC_000019.9:g.6709697T>A , CM000681.1:g.6709697T>A	GRCh37
NC_000019.8:g.6660697T>A	NCBI36
NG_009557.1:g.15966A>T , LRG_27:g.15966A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000695652.1:c.1720A>T	ENSP00000512083.1:p.Lys574Ter
ENST00000695654.1:c.967A>T	ENSP00000512085.1:p.Lys323Ter
ENST00000695655.1:c.784A>T	ENSP00000512086.1:n.784A>T
ENST00000695692.1:n.1207A>T
ENST00000245907.11:c.1843A>T MANE Select	ENSP00000245907.4:p.Lys615Ter
ENST00000245907.10:c.1843A>T	ENSP00000245907.4:p.Lys615Ter
NM_000064.3:c.1843A>T	NP_000055.2:p.Lys615Ter
NM_000064.4:c.1843A>T MANE Select	NP_000055.2:p.Lys615Ter