Canonical Allele Identifier: CA2587878797
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs2145432743
gnomAD v4: 19-6714577-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6714577C>G , CM000681.2:g.6714577C>G GRCh38
NC_000019.9:g.6714588C>G , CM000681.1:g.6714588C>G GRCh37
NC_000019.8:g.6665588C>G NCBI36
NG_009557.1:g.11075G>C , LRG_27:g.11075G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.382-131G>C ENSP00000512083.1:n.382-131G>C
ENST00000245907.11:c.505-131G>C MANE Select ENSP00000245907.4:n.505-131G>C
ENST00000245907.10:c.505-131G>C ENSP00000245907.4:n.505-131G>C
NM_000064.3:c.505-131G>C NP_000055.2:n.505-131G>C
NM_000064.4:c.505-131G>C MANE Select NP_000055.2:n.505-131G>C
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