Canonical Allele Identifier: CA1272472153
Gene: DUSP2 HGNC NCBI

Linked Data

dbSNP Id: rs115786506
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96143276G>C , CM000664.2:g.96143276G>C GRCh38
NC_000002.11:g.96809015G>C , CM000664.1:g.96809015G>C GRCh37
NC_000002.10:g.96172742G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000288943.5:c.*547C>G MANE Select ENSP00000288943.4:n.*547C>G
ENST00000288943.4:c.*547C>G ENSP00000288943.4:n.*547C>G
NM_004418.3:c.*547C>G NP_004409.1:n.*547C>G
XM_017003546.1:c.*547C>G XP_016859035.1:n.*547C>G
NM_004418.4:c.*547C>G MANE Select NP_004409.1:n.*547C>G
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