Canonical Allele Identifier: CA1272472293
Gene: DUSP2 HGNC NCBI

Linked Data

dbSNP Id: rs1573921764
gnomAD v4: 2-96143601-A-C
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000288943.5:c.*222T>G MANE Select ENSP00000288943.4:n.*222T>G
ENST00000288943.4:c.*222T>G ENSP00000288943.4:n.*222T>G
NM_004418.3:c.*222T>G NP_004409.1:n.*222T>G
XM_017003546.1:c.*222T>G XP_016859035.1:n.*222T>G
NM_004418.4:c.*222T>G MANE Select NP_004409.1:n.*222T>G
Search 100 bp 5'
Search 100 bp 3'