Canonical Allele Identifier: CA52376882
Gene: DUSP2 HGNC NCBI

Linked Data

dbSNP Id: rs111938402
gnomAD v4: 2-96143605-C-G
MyVariant Identifiers: chr2:g.96809344C>G (hg19) chr2:g.96143605C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96143605C>G , CM000664.2:g.96143605C>G GRCh38
NC_000002.11:g.96809344C>G , CM000664.1:g.96809344C>G GRCh37
NC_000002.10:g.96173071C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000288943.5:c.*218G>C MANE Select ENSP00000288943.4:n.*218G>C
ENST00000288943.4:c.*218G>C ENSP00000288943.4:n.*218G>C
NM_004418.3:c.*218G>C NP_004409.1:n.*218G>C
XM_017003546.1:c.*218G>C XP_016859035.1:n.*218G>C
NM_004418.4:c.*218G>C MANE Select NP_004409.1:n.*218G>C
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