Canonical Allele Identifier: CA2320568169
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs1599525242
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713778C>T , CM000681.2:g.6713778C>T GRCh38
NC_000019.9:g.6713789C>T , CM000681.1:g.6713789C>T GRCh37
NC_000019.8:g.6664789C>T NCBI36
NG_009557.1:g.11874G>A , LRG_27:g.11874G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.650+214G>A ENSP00000512083.1:n.650+214G>A
ENST00000245907.11:c.773+214G>A MANE Select ENSP00000245907.4:n.773+214G>A
ENST00000245907.10:c.773+214G>A ENSP00000245907.4:n.773+214G>A
ENST00000595577.1:n.277+214G>A
ENST00000597442.5:n.11G>A
NM_000064.3:c.773+214G>A NP_000055.2:n.773+214G>A
NM_000064.4:c.773+214G>A MANE Select NP_000055.2:n.773+214G>A
Search 100 bp 5'
Search 100 bp 3'