Canonical Allele Identifier: CA2660167698
Gene: DUSP2 HGNC NCBI

Linked Data

gnomAD v4: 2-96143594-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96143594G>T , CM000664.2:g.96143594G>T GRCh38
NC_000002.11:g.96809333G>T , CM000664.1:g.96809333G>T GRCh37
NC_000002.10:g.96173060G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000288943.5:c.*229C>A MANE Select ENSP00000288943.4:n.*229C>A
ENST00000288943.4:c.*229C>A ENSP00000288943.4:n.*229C>A
NM_004418.3:c.*229C>A NP_004409.1:n.*229C>A
XM_017003546.1:c.*229C>A XP_016859035.1:n.*229C>A
NM_004418.4:c.*229C>A MANE Select NP_004409.1:n.*229C>A
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