Canonical Allele Identifier: CA403643247
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6714235T>A , CM000681.2:g.6714235T>A GRCh38
NC_000019.9:g.6714246T>A , CM000681.1:g.6714246T>A GRCh37
NC_000019.8:g.6665246T>A NCBI36
NG_009557.1:g.11417A>T , LRG_27:g.11417A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.490A>T ENSP00000512083.1:p.Lys164Ter
ENST00000245907.11:c.613A>T MANE Select ENSP00000245907.4:p.Lys205Ter
ENST00000245907.10:c.613A>T ENSP00000245907.4:p.Lys205Ter
ENST00000595577.1:n.117A>T
NM_000064.3:c.613A>T NP_000055.2:p.Lys205Ter
NM_000064.4:c.613A>T MANE Select NP_000055.2:p.Lys205Ter