Canonical Allele Identifier: CA403618337

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6685035G>C (hg19) ; chr19:g.6685024G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6685024G>C , CM000681.2:g.6685024G>C	GRCh38
NC_000019.9:g.6685035G>C , CM000681.1:g.6685035G>C	GRCh37
NC_000019.8:g.6636035G>C	NCBI36
NG_009557.1:g.40628C>G , LRG_27:g.40628C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2281C>G
ENST00000695653.1:c.1842C>G	ENSP00000512084.1:p.Ile614Met
ENST00000695654.1:c.2958C>G	ENSP00000512085.1:p.Ile986Met
ENST00000695690.1:n.124C>G
ENST00000695691.1:n.124C>G
ENST00000245907.11:c.3933C>G MANE Select	ENSP00000245907.4:p.Ile1311Met
ENST00000245907.10:c.3933C>G	ENSP00000245907.4:p.Ile1311Met
ENST00000596238.1:n.376C>G
ENST00000596548.1:c.15C>G	ENSP00000469744.1:p.Ile5Met
ENST00000601008.1:c.241+1722C>G	ENSP00000471384.1:n.241+1722C>G
NM_000064.3:c.3933C>G	NP_000055.2:p.Ile1311Met
NM_000064.4:c.3933C>G MANE Select	NP_000055.2:p.Ile1311Met