Canonical Allele Identifier: CA1272472215
Gene: DUSP2 HGNC NCBI

Linked Data

dbSNP Id: rs1682439696
gnomAD v4: 2-96143436-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96143436G>A , CM000664.2:g.96143436G>A GRCh38
NC_000002.11:g.96809175G>A , CM000664.1:g.96809175G>A GRCh37
NC_000002.10:g.96172902G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000288943.5:c.*387C>T MANE Select ENSP00000288943.4:n.*387C>T
ENST00000288943.4:c.*387C>T ENSP00000288943.4:n.*387C>T
NM_004418.3:c.*387C>T NP_004409.1:n.*387C>T
XM_017003546.1:c.*387C>T XP_016859035.1:n.*387C>T
NM_004418.4:c.*387C>T MANE Select NP_004409.1:n.*387C>T