Canonical Allele Identifier: CA2320568409
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs1967981652
gnomAD v4: 19-6714105-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6714105G>A , CM000681.2:g.6714105G>A GRCh38
NC_000019.9:g.6714116G>A , CM000681.1:g.6714116G>A GRCh37
NC_000019.8:g.6665116G>A NCBI36
NG_009557.1:g.11547C>T , LRG_27:g.11547C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.560-23C>T ENSP00000512083.1:n.560-23C>T
ENST00000245907.11:c.683-23C>T MANE Select ENSP00000245907.4:n.683-23C>T
ENST00000245907.10:c.683-23C>T ENSP00000245907.4:n.683-23C>T
ENST00000595577.1:n.187-23C>T
NM_000064.3:c.683-23C>T NP_000055.2:n.683-23C>T
NM_000064.4:c.683-23C>T MANE Select NP_000055.2:n.683-23C>T
Search 100 bp 5'
Search 100 bp 3'