Canonical Allele Identifier: CA2587875417
Gene: C3 HGNC NCBI

Linked Data

gnomAD v4: 19-6697823-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6697823G>T , CM000681.2:g.6697823G>T GRCh38
NC_000019.9:g.6697834G>T , CM000681.1:g.6697834G>T GRCh37
NC_000019.8:g.6648834G>T NCBI36
NG_009557.1:g.27829C>A , LRG_27:g.27829C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000695651.1:n.789-29C>A
ENST00000695652.1:c.2318-29C>A ENSP00000512083.1:n.2318-29C>A
ENST00000695653.1:c.350-29C>A ENSP00000512084.1:n.350-29C>A
ENST00000695654.1:c.1565-29C>A ENSP00000512085.1:n.1565-29C>A
ENST00000695655.1:c.1382-29C>A ENSP00000512086.1:n.1382-29C>A
ENST00000695692.1:n.1805-29C>A
ENST00000245907.11:c.2441-29C>A MANE Select ENSP00000245907.4:n.2441-29C>A
ENST00000245907.10:c.2441-29C>A ENSP00000245907.4:n.2441-29C>A
ENST00000602053.1:n.489-29C>A
NM_000064.3:c.2441-29C>A NP_000055.2:n.2441-29C>A
NM_000064.4:c.2441-29C>A MANE Select NP_000055.2:n.2441-29C>A
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