Canonical Allele Identifier: CA9129707
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs753744978
gnomAD v2: 19-6714080-G-A
gnomAD v3: 19-6714069-G-A
gnomAD v4: 19-6714069-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6714069G>A , CM000681.2:g.6714069G>A GRCh38
NC_000019.9:g.6714080G>A , CM000681.1:g.6714080G>A GRCh37
NC_000019.8:g.6665080G>A NCBI36
NG_009557.1:g.11583C>T , LRG_27:g.11583C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.573C>T ENSP00000512083.1:p.Phe191=
ENST00000245907.11:c.696C>T MANE Select ENSP00000245907.4:p.Phe232=
ENST00000245907.10:c.696C>T ENSP00000245907.4:p.Phe232=
ENST00000595577.1:n.200C>T
NM_000064.3:c.696C>T NP_000055.2:p.Phe232=
NM_000064.4:c.696C>T MANE Select NP_000055.2:p.Phe232=