Canonical Allele Identifier: CA403642653

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6713476A>G (hg19) ; chr19:g.6713465A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713465A>G , CM000681.2:g.6713465A>G	GRCh38
NC_000019.9:g.6713476A>G , CM000681.1:g.6713476A>G	GRCh37
NC_000019.8:g.6664476A>G	NCBI36
NG_009557.1:g.12187T>C , LRG_27:g.12187T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.695T>C	ENSP00000512083.1:p.Phe232Ser
ENST00000695692.1:n.142T>C
ENST00000245907.11:c.818T>C MANE Select	ENSP00000245907.4:p.Phe273Ser
ENST00000245907.10:c.818T>C	ENSP00000245907.4:p.Phe273Ser
ENST00000595577.1:n.322T>C
ENST00000597442.5:n.68T>C
NM_000064.3:c.818T>C	NP_000055.2:p.Phe273Ser
NM_000064.4:c.818T>C MANE Select	NP_000055.2:p.Phe273Ser