Canonical Allele Identifier: CA631722520
Gene: C3 HGNC NCBI

Linked Data

gnomAD v2: 19-6709645-A-G
gnomAD v4: 19-6709634-A-G
MyVariant Identifiers: chr19:g.6709645_6709646delinsGG (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6709634A>G , CM000681.2:g.6709634A>G GRCh38
NC_000019.9:g.6709645A>G , CM000681.1:g.6709645A>G GRCh37
NC_000019.8:g.6660645A>G NCBI36
NG_009557.1:g.16018T>C , LRG_27:g.16018T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000695652.1:c.1722+50T>C ENSP00000512083.1:n.1722+50T>C
ENST00000695654.1:c.969+50T>C ENSP00000512085.1:n.969+50T>C
ENST00000695655.1:c.786+50T>C ENSP00000512086.1:n.786+50T>C
ENST00000695692.1:n.1209+50T>C
ENST00000245907.11:c.1845+50T>C MANE Select ENSP00000245907.4:n.1845+50T>C
ENST00000245907.10:c.1845+50T>C ENSP00000245907.4:n.1845+50T>C
NM_000064.3:c.1845+50T>C NP_000055.2:n.1845+50T>C
NM_000064.4:c.1845+50T>C MANE Select NP_000055.2:n.1845+50T>C
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