Canonical Allele Identifier: CA1272472294
Gene: DUSP2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96143601A= , CM000664.2:g.96143601A= GRCh38
NC_000002.11:g.96809340A= , CM000664.1:g.96809340A= GRCh37
NC_000002.10:g.96173067A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000288943.5:c.*222T= MANE Select ENSP00000288943.4:n.*222T=
ENST00000288943.4:c.*222T= ENSP00000288943.4:n.*222T=
NM_004418.3:c.*222T= NP_004409.1:n.*222T=
XM_017003546.1:c.*222T= XP_016859035.1:n.*222T=
NM_004418.4:c.*222T= MANE Select NP_004409.1:n.*222T=
Search 100 bp 5'
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