Canonical Allele Identifier: CA895754157
Gene: DUSP2 HGNC NCBI

Linked Data

dbSNP Id: rs1462263813
MyVariant Identifiers: chr2:g.96809124T>A (hg19) chr2:g.96143385T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96143385T>A , CM000664.2:g.96143385T>A GRCh38
NC_000002.11:g.96809124T>A , CM000664.1:g.96809124T>A GRCh37
NC_000002.10:g.96172851T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000288943.5:c.*438A>T MANE Select ENSP00000288943.4:n.*438A>T
ENST00000288943.4:c.*438A>T ENSP00000288943.4:n.*438A>T
NM_004418.3:c.*438A>T NP_004409.1:n.*438A>T
XM_017003546.1:c.*438A>T XP_016859035.1:n.*438A>T
NM_004418.4:c.*438A>T MANE Select NP_004409.1:n.*438A>T
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