Canonical Allele Identifier: CA2660167719
Gene: DUSP2 HGNC NCBI

Linked Data

gnomAD v4: 2-96143604-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96143604C>T , CM000664.2:g.96143604C>T GRCh38
NC_000002.11:g.96809343C>T , CM000664.1:g.96809343C>T GRCh37
NC_000002.10:g.96173070C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000288943.5:c.*219G>A MANE Select ENSP00000288943.4:n.*219G>A
ENST00000288943.4:c.*219G>A ENSP00000288943.4:n.*219G>A
NM_004418.3:c.*219G>A NP_004409.1:n.*219G>A
XM_017003546.1:c.*219G>A XP_016859035.1:n.*219G>A
NM_004418.4:c.*219G>A MANE Select NP_004409.1:n.*219G>A
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