Canonical Allele Identifier: CA403618264

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6685018C>G (hg19) ; chr19:g.6685007C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6685007C>G , CM000681.2:g.6685007C>G	GRCh38
NC_000019.9:g.6685018C>G , CM000681.1:g.6685018C>G	GRCh37
NC_000019.8:g.6636018C>G	NCBI36
NG_009557.1:g.40645G>C , LRG_27:g.40645G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2298G>C
ENST00000695653.1:c.1859G>C	ENSP00000512084.1:p.Ser620Thr
ENST00000695654.1:c.2975G>C	ENSP00000512085.1:p.Ser992Thr
ENST00000695690.1:n.141G>C
ENST00000695691.1:n.141G>C
ENST00000245907.11:c.3950G>C MANE Select	ENSP00000245907.4:p.Ser1317Thr
ENST00000245907.10:c.3950G>C	ENSP00000245907.4:p.Ser1317Thr
ENST00000596238.1:n.393G>C
ENST00000596548.1:c.32G>C	ENSP00000469744.1:p.Ser11Thr
ENST00000601008.1:c.241+1739G>C	ENSP00000471384.1:n.241+1739G>C
NM_000064.3:c.3950G>C	NP_000055.2:p.Ser1317Thr
NM_000064.4:c.3950G>C MANE Select	NP_000055.2:p.Ser1317Thr