Canonical Allele Identifier: CA895754213
Gene: DUSP2 HGNC NCBI

Linked Data

dbSNP Id: rs1328323000
gnomAD v4: 2-96143593-G-A
MyVariant Identifiers: chr2:g.96809332G>A (hg19) chr2:g.96143593G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96143593G>A , CM000664.2:g.96143593G>A GRCh38
NC_000002.11:g.96809332G>A , CM000664.1:g.96809332G>A GRCh37
NC_000002.10:g.96173059G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000288943.5:c.*230C>T MANE Select ENSP00000288943.4:n.*230C>T
ENST00000288943.4:c.*230C>T ENSP00000288943.4:n.*230C>T
NM_004418.3:c.*230C>T NP_004409.1:n.*230C>T
XM_017003546.1:c.*230C>T XP_016859035.1:n.*230C>T
NM_004418.4:c.*230C>T MANE Select NP_004409.1:n.*230C>T
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