Canonical Allele Identifier: CA403642699
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713475A>G , CM000681.2:g.6713475A>G GRCh38
NC_000019.9:g.6713486A>G , CM000681.1:g.6713486A>G GRCh37
NC_000019.8:g.6664486A>G NCBI36
NG_009557.1:g.12177T>C , LRG_27:g.12177T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.685T>C ENSP00000512083.1:p.Phe229Leu
ENST00000695692.1:n.132T>C
ENST00000245907.11:c.808T>C MANE Select ENSP00000245907.4:p.Phe270Leu
ENST00000245907.10:c.808T>C ENSP00000245907.4:p.Phe270Leu
ENST00000595577.1:n.312T>C
ENST00000597442.5:n.58T>C
NM_000064.3:c.808T>C NP_000055.2:p.Phe270Leu
NM_000064.4:c.808T>C MANE Select NP_000055.2:p.Phe270Leu