Canonical Allele Identifier: CA1272472295
Gene: DUSP2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96143605C= , CM000664.2:g.96143605C= GRCh38
NC_000002.11:g.96809344C= , CM000664.1:g.96809344C= GRCh37
NC_000002.10:g.96173071C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000288943.5:c.*218G= MANE Select ENSP00000288943.4:n.*218G=
ENST00000288943.4:c.*218G= ENSP00000288943.4:n.*218G=
NM_004418.3:c.*218G= NP_004409.1:n.*218G=
XM_017003546.1:c.*218G= XP_016859035.1:n.*218G=
NM_004418.4:c.*218G= MANE Select NP_004409.1:n.*218G=
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