Canonical Allele Identifier: CA2320568255
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs1599525355
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713863T>C , CM000681.2:g.6713863T>C GRCh38
NC_000019.9:g.6713874T>C , CM000681.1:g.6713874T>C GRCh37
NC_000019.8:g.6664874T>C NCBI36
NG_009557.1:g.11789A>G , LRG_27:g.11789A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.650+129A>G ENSP00000512083.1:n.650+129A>G
ENST00000245907.11:c.773+129A>G MANE Select ENSP00000245907.4:n.773+129A>G
ENST00000245907.10:c.773+129A>G ENSP00000245907.4:n.773+129A>G
ENST00000595577.1:n.277+129A>G
NM_000064.3:c.773+129A>G NP_000055.2:n.773+129A>G
NM_000064.4:c.773+129A>G MANE Select NP_000055.2:n.773+129A>G
Search 100 bp 5'
Search 100 bp 3'