Canonical Allele Identifier: CA1272472289
Gene: DUSP2 HGNC NCBI

Linked Data

dbSNP Id: rs1724120
gnomAD v4: 2-96143592-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96143592T>A , CM000664.2:g.96143592T>A GRCh38
NC_000002.11:g.96809331T>A , CM000664.1:g.96809331T>A GRCh37
NC_000002.10:g.96173058T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000288943.5:c.*231A>T MANE Select ENSP00000288943.4:n.*231A>T
ENST00000288943.4:c.*231A>T ENSP00000288943.4:n.*231A>T
NM_004418.3:c.*231A>T NP_004409.1:n.*231A>T
XM_017003546.1:c.*231A>T XP_016859035.1:n.*231A>T
NM_004418.4:c.*231A>T MANE Select NP_004409.1:n.*231A>T
Search 100 bp 5'
Search 100 bp 3'