Canonical Allele Identifier: CA884132236
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs776459204
gnomAD v3: 19-6714126-G-T
gnomAD v4: 19-6714126-G-T
MyVariant Identifiers: chr19:g.6714137G>T (hg19) chr19:g.6714126G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6714126G>T , CM000681.2:g.6714126G>T GRCh38
NC_000019.9:g.6714137G>T , CM000681.1:g.6714137G>T GRCh37
NC_000019.8:g.6665137G>T NCBI36
NG_009557.1:g.11526C>A , LRG_27:g.11526C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000695652.1:c.559+40C>A ENSP00000512083.1:n.559+40C>A
ENST00000245907.11:c.682+40C>A MANE Select ENSP00000245907.4:n.682+40C>A
ENST00000245907.10:c.682+40C>A ENSP00000245907.4:n.682+40C>A
ENST00000595577.1:n.186+40C>A
NM_000064.3:c.682+40C>A NP_000055.2:n.682+40C>A
NM_000064.4:c.682+40C>A MANE Select NP_000055.2:n.682+40C>A
Search 100 bp 5'
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