Canonical Allele Identifier: CA884132225
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs1232145585
MyVariant Identifiers: chr19:g.6714115_6714116insGGGGCCGGCGC (hg19) chr19:g.6714104_6714105insGGGGCCGGCGC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6714105_6714115dup , CM000681.2:g.6714105_6714115dup GRCh38
NC_000019.9:g.6714116_6714126dup , CM000681.1:g.6714116_6714126dup GRCh37
NC_000019.8:g.6665116_6665126dup NCBI36
NG_009557.1:g.11537_11547dup , LRG_27:g.11537_11547dup

Transcript Alleles

HGVS Amino-acid change
ENST00000695652.1:c.560-33_560-23dup ENSP00000512083.1:n.560-33_560-23dup
ENST00000245907.11:c.683-33_683-23dup MANE Select ENSP00000245907.4:n.683-33_683-23dup
ENST00000245907.10:c.683-33_683-23dup ENSP00000245907.4:n.683-33_683-23dup
ENST00000595577.1:n.187-33_187-23dup
NM_000064.3:c.683-33_683-23dup NP_000055.2:n.683-33_683-23dup
NM_000064.4:c.683-33_683-23dup MANE Select NP_000055.2:n.683-33_683-23dup
Search 100 bp 5'
Search 100 bp 3'