Canonical Allele Identifier: CA2587878662
Gene: C3 HGNC NCBI

Linked Data

gnomAD v4: 19-6714146-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6714146C>A , CM000681.2:g.6714146C>A GRCh38
NC_000019.9:g.6714157C>A , CM000681.1:g.6714157C>A GRCh37
NC_000019.8:g.6665157C>A NCBI36
NG_009557.1:g.11506G>T , LRG_27:g.11506G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.559+20G>T ENSP00000512083.1:n.559+20G>T
ENST00000245907.11:c.682+20G>T MANE Select ENSP00000245907.4:n.682+20G>T
ENST00000245907.10:c.682+20G>T ENSP00000245907.4:n.682+20G>T
ENST00000595577.1:n.186+20G>T
NM_000064.3:c.682+20G>T NP_000055.2:n.682+20G>T
NM_000064.4:c.682+20G>T MANE Select NP_000055.2:n.682+20G>T
Search 100 bp 5'
Search 100 bp 3'