Canonical Allele Identifier: CA884131914
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs1236039103
gnomAD v4: 19-6713870-A-AC
MyVariant Identifiers: chr19:g.6713881_6713882insC (hg19) chr19:g.6713870_6713871insC (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713875dup , CM000681.2:g.6713875dup GRCh38
NC_000019.9:g.6713886dup , CM000681.1:g.6713886dup GRCh37
NC_000019.8:g.6664886dup NCBI36
NG_009557.1:g.11781dup , LRG_27:g.11781dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.650+121dup ENSP00000512083.1:n.650+121dup
ENST00000245907.11:c.773+121dup MANE Select ENSP00000245907.4:n.773+121dup
ENST00000245907.10:c.773+121dup ENSP00000245907.4:n.773+121dup
ENST00000595577.1:n.277+121dup
NM_000064.3:c.773+121dup NP_000055.2:n.773+121dup
NM_000064.4:c.773+121dup MANE Select NP_000055.2:n.773+121dup
Search 100 bp 5'
Search 100 bp 3'