Canonical Allele Identifier: CA2320568420
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs1599525643

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6714117G>A , CM000681.2:g.6714117G>A GRCh38
NC_000019.9:g.6714128G>A , CM000681.1:g.6714128G>A GRCh37
NC_000019.8:g.6665128G>A NCBI36
NG_009557.1:g.11535C>T , LRG_27:g.11535C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000695652.1:c.560-35C>T ENSP00000512083.1:n.560-35C>T
ENST00000245907.11:c.683-35C>T MANE Select ENSP00000245907.4:n.683-35C>T
ENST00000245907.10:c.683-35C>T ENSP00000245907.4:n.683-35C>T
ENST00000595577.1:n.187-35C>T
NM_000064.3:c.683-35C>T NP_000055.2:n.683-35C>T
NM_000064.4:c.683-35C>T MANE Select NP_000055.2:n.683-35C>T