Canonical Allele Identifier: CA403618264
Gene: C3 HGNC NCBI

Linked Data

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