Canonical Allele Identifier: CA403640721
Gene: C3 HGNC NCBI

Linked Data

gnomAD v4: 19-6710840-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6710840C>A , CM000681.2:g.6710840C>A GRCh38
NC_000019.9:g.6710851C>A , CM000681.1:g.6710851C>A GRCh37
NC_000019.8:g.6661851C>A NCBI36
NG_009557.1:g.14812G>T , LRG_27:g.14812G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000695652.1:c.1362G>T ENSP00000512083.1:p.Met454Ile
ENST00000695654.1:c.609G>T ENSP00000512085.1:p.Met203Ile
ENST00000695655.1:c.390G>T ENSP00000512086.1:p.Met130Ile
ENST00000695692.1:n.849G>T
ENST00000245907.11:c.1485G>T MANE Select ENSP00000245907.4:p.Met495Ile
ENST00000245907.10:c.1485G>T ENSP00000245907.4:p.Met495Ile
ENST00000600763.1:n.118G>T
NM_000064.3:c.1485G>T NP_000055.2:p.Met495Ile
NM_000064.4:c.1485G>T MANE Select NP_000055.2:p.Met495Ile