Canonical Allele Identifier: CA895754123
Gene: DUSP2 HGNC NCBI

Linked Data

dbSNP Id: rs777794683
gnomAD v3: 2-96143308-A-C
gnomAD v4: 2-96143308-A-C
MyVariant Identifiers: chr2:g.96809047A>C (hg19) chr2:g.96143308A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96143308A>C , CM000664.2:g.96143308A>C GRCh38
NC_000002.11:g.96809047A>C , CM000664.1:g.96809047A>C GRCh37
NC_000002.10:g.96172774A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000288943.5:c.*515T>G MANE Select ENSP00000288943.4:n.*515T>G
ENST00000288943.4:c.*515T>G ENSP00000288943.4:n.*515T>G
NM_004418.3:c.*515T>G NP_004409.1:n.*515T>G
XM_017003546.1:c.*515T>G XP_016859035.1:n.*515T>G
NM_004418.4:c.*515T>G MANE Select NP_004409.1:n.*515T>G
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