Canonical Allele Identifier: CA895754126
Gene: DUSP2 HGNC NCBI

Linked Data

dbSNP Id: rs1382738210
gnomAD v3: 2-96143318-C-T
gnomAD v4: 2-96143318-C-T
MyVariant Identifiers: chr2:g.96809057C>T (hg19) chr2:g.96143318C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96143318C>T , CM000664.2:g.96143318C>T GRCh38
NC_000002.11:g.96809057C>T , CM000664.1:g.96809057C>T GRCh37
NC_000002.10:g.96172784C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000288943.5:c.*505G>A MANE Select ENSP00000288943.4:n.*505G>A
ENST00000288943.4:c.*505G>A ENSP00000288943.4:n.*505G>A
NM_004418.3:c.*505G>A NP_004409.1:n.*505G>A
XM_017003546.1:c.*505G>A XP_016859035.1:n.*505G>A
NM_004418.4:c.*505G>A MANE Select NP_004409.1:n.*505G>A
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