Canonical Allele Identifier: CA2660167252
Gene: DUSP2 HGNC NCBI

Linked Data

gnomAD v4: 2-96143312-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96143312T>G , CM000664.2:g.96143312T>G GRCh38
NC_000002.11:g.96809051T>G , CM000664.1:g.96809051T>G GRCh37
NC_000002.10:g.96172778T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000288943.5:c.*511A>C MANE Select ENSP00000288943.4:n.*511A>C
ENST00000288943.4:c.*511A>C ENSP00000288943.4:n.*511A>C
NM_004418.3:c.*511A>C NP_004409.1:n.*511A>C
XM_017003546.1:c.*511A>C XP_016859035.1:n.*511A>C
NM_004418.4:c.*511A>C MANE Select NP_004409.1:n.*511A>C
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