Canonical Allele Identifier: CA1272472142
Gene: DUSP2 HGNC NCBI

Linked Data

dbSNP Id: rs1682436184

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96143246C>A , CM000664.2:g.96143246C>A GRCh38
NC_000002.11:g.96808985C>A , CM000664.1:g.96808985C>A GRCh37
NC_000002.10:g.96172712C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000288943.5:c.*577G>T MANE Select ENSP00000288943.4:n.*577G>T
ENST00000288943.4:c.*577G>T ENSP00000288943.4:n.*577G>T
NM_004418.3:c.*577G>T NP_004409.1:n.*577G>T
XM_017003546.1:c.*577G>T XP_016859035.1:n.*577G>T
NM_004418.4:c.*577G>T MANE Select NP_004409.1:n.*577G>T