Canonical Allele Identifier: CA884131763
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs1418833733
gnomAD v3: 19-6713758-G-GC
gnomAD v4: 19-6713758-G-GC
MyVariant Identifiers: chr19:g.6713769_6713770insC (hg19) chr19:g.6713758_6713759insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713763dup , CM000681.2:g.6713763dup GRCh38
NC_000019.9:g.6713774dup , CM000681.1:g.6713774dup GRCh37
NC_000019.8:g.6664774dup NCBI36
NG_009557.1:g.11893dup , LRG_27:g.11893dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.650+233dup ENSP00000512083.1:n.650+233dup
ENST00000245907.11:c.773+233dup MANE Select ENSP00000245907.4:n.773+233dup
ENST00000245907.10:c.773+233dup ENSP00000245907.4:n.773+233dup
ENST00000595577.1:n.277+233dup
ENST00000597442.5:n.23+7dup
NM_000064.3:c.773+233dup NP_000055.2:n.773+233dup
NM_000064.4:c.773+233dup MANE Select NP_000055.2:n.773+233dup
Search 100 bp 5'
Search 100 bp 3'