Canonical Allele Identifier: CA505124995

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6714220T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6714209T>A , CM000681.2:g.6714209T>A	GRCh38
NC_000019.9:g.6714220T>A , CM000681.1:g.6714220T>A	GRCh37
NC_000019.8:g.6665220T>A	NCBI36
NG_009557.1:g.11443A>T , LRG_27:g.11443A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.516A>T	ENSP00000512083.1:p.Ser172=
ENST00000245907.11:c.639A>T MANE Select	ENSP00000245907.4:p.Ser213=
ENST00000245907.10:c.639A>T	ENSP00000245907.4:p.Ser213=
ENST00000595577.1:n.143A>T
NM_000064.3:c.639A>T	NP_000055.2:p.Ser213=
NM_000064.4:c.639A>T MANE Select	NP_000055.2:p.Ser213=