Canonical Allele Identifier: CA2320568077
Gene: C3 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713683T= , CM000681.2:g.6713683T= GRCh38
NC_000019.9:g.6713694T= , CM000681.1:g.6713694T= GRCh37
NC_000019.8:g.6664694T= NCBI36
NG_009557.1:g.11969A= , LRG_27:g.11969A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.651-174A= ENSP00000512083.1:n.651-174A=
ENST00000245907.11:c.774-174A= MANE Select ENSP00000245907.4:n.774-174A=
ENST00000245907.10:c.774-174A= ENSP00000245907.4:n.774-174A=
ENST00000595577.1:n.278-174A=
ENST00000597442.5:n.23+83A=
NM_000064.3:c.774-174A= NP_000055.2:n.774-174A=
NM_000064.4:c.774-174A= MANE Select NP_000055.2:n.774-174A=
Search 100 bp 5'
Search 100 bp 3'