Canonical Allele Identifier: CA1619357964
Gene: C2 HGNC NCBI

Linked Data

dbSNP Id: rs1767587918
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31904506dup , CM000668.2:g.31904506dup GRCh38
NC_000006.11:g.31872283dup , CM000668.1:g.31872283dup GRCh37
NC_000006.10:g.31980262dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000452323.7:c.73+3367dup ENSP00000392322.2:n.73+3367dup
ENST00000497706.6:c.-64+6564dup ENSP00000417482.2:n.-64+6564dup
ENST00000695637.1:c.-360+6231dup ENSP00000512074.1:n.-360+6231dup
ENST00000452202.5:c.73+3367dup ENSP00000406121.1:n.73+3367dup
ENST00000452323.6:c.73+3367dup ENSP00000392322.2:n.73+3367dup
ENST00000469372.5:c.-64+6564dup ENSP00000418923.1:n.-64+6564dup
ENST00000497706.5:c.-64+6564dup ENSP00000417482.1:n.-64+6564dup
NM_001178063.2:c.73+3367dup NP_001171534.1:n.73+3367dup
NM_001282457.1:c.-64+6564dup NP_001269386.1:n.-64+6564dup
NM_001282457.2:c.-64+6564dup NP_001269386.1:n.-64+6564dup
NM_001178063.3:c.73+3367dup NP_001171534.1:n.73+3367dup
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