Canonical Allele Identifier: CA2660167178
Gene: DUSP2 HGNC NCBI

Linked Data

gnomAD v4: 2-96143241-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96143241C>G , CM000664.2:g.96143241C>G GRCh38
NC_000002.11:g.96808980C>G , CM000664.1:g.96808980C>G GRCh37
NC_000002.10:g.96172707C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000288943.5:c.*582G>C MANE Select ENSP00000288943.4:n.*582G>C
ENST00000288943.4:c.*582G>C ENSP00000288943.4:n.*582G>C
NM_004418.3:c.*582G>C NP_004409.1:n.*582G>C
XM_017003546.1:c.*582G>C XP_016859035.1:n.*582G>C
NM_004418.4:c.*582G>C MANE Select NP_004409.1:n.*582G>C