Canonical Allele Identifier: CA403640742
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6710845T>A , CM000681.2:g.6710845T>A GRCh38
NC_000019.9:g.6710856T>A , CM000681.1:g.6710856T>A GRCh37
NC_000019.8:g.6661856T>A NCBI36
NG_009557.1:g.14807A>T , LRG_27:g.14807A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000695652.1:c.1357A>T ENSP00000512083.1:p.Ile453Phe
ENST00000695654.1:c.604A>T ENSP00000512085.1:p.Ile202Phe
ENST00000695655.1:c.385A>T ENSP00000512086.1:p.Ile129Phe
ENST00000695692.1:n.844A>T
ENST00000245907.11:c.1480A>T MANE Select ENSP00000245907.4:p.Ile494Phe
ENST00000245907.10:c.1480A>T ENSP00000245907.4:p.Ile494Phe
ENST00000600763.1:n.113A>T
NM_000064.3:c.1480A>T NP_000055.2:p.Ile494Phe
NM_000064.4:c.1480A>T MANE Select NP_000055.2:p.Ile494Phe