Canonical Allele Identifier: CA403618682

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6685153G>C (hg19) ; chr19:g.6685142G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6685142G>C , CM000681.2:g.6685142G>C	GRCh38
NC_000019.9:g.6685153G>C , CM000681.1:g.6685153G>C	GRCh37
NC_000019.8:g.6636153G>C	NCBI36
NG_009557.1:g.40510C>G , LRG_27:g.40510C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2163C>G
ENST00000695653.1:c.1724C>G	ENSP00000512084.1:p.Thr575Ser
ENST00000695654.1:c.2840C>G	ENSP00000512085.1:p.Thr947Ser
ENST00000695690.1:n.6C>G
ENST00000695691.1:n.6C>G
ENST00000245907.11:c.3815C>G MANE Select	ENSP00000245907.4:p.Thr1272Ser
ENST00000245907.10:c.3815C>G	ENSP00000245907.4:p.Thr1272Ser
ENST00000596238.1:n.258C>G
ENST00000601008.1:c.241+1604C>G	ENSP00000471384.1:n.241+1604C>G
NM_000064.3:c.3815C>G	NP_000055.2:p.Thr1272Ser
NM_000064.4:c.3815C>G MANE Select	NP_000055.2:p.Thr1272Ser