Canonical Allele Identifier: CA2660167711
Gene: DUSP2 HGNC NCBI

Linked Data

gnomAD v4: 2-96143601-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96143601A>G , CM000664.2:g.96143601A>G GRCh38
NC_000002.11:g.96809340A>G , CM000664.1:g.96809340A>G GRCh37
NC_000002.10:g.96173067A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000288943.5:c.*222T>C MANE Select ENSP00000288943.4:n.*222T>C
ENST00000288943.4:c.*222T>C ENSP00000288943.4:n.*222T>C
NM_004418.3:c.*222T>C NP_004409.1:n.*222T>C
XM_017003546.1:c.*222T>C XP_016859035.1:n.*222T>C
NM_004418.4:c.*222T>C MANE Select NP_004409.1:n.*222T>C
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