Canonical Allele Identifier: CA11075636
Gene: DUSP2 HGNC NCBI
MyVariant.info:
GRCh38 chr2:g.96143592T>C
GRCh37 chr2:g.96809331T>C
gnomAD v2:
2:96809331 T / C
gnomAD v3:
2:96143592 T / C
gnomAD v4:
chr2-96143592-T-C
Joint Max Group AF 0.75201685 (EAS)
Genomes Max Group AF 0.77616083 (EAS)
Exomes Max Group AF 0.74483611 (EAS)
dbSNP:
1724120
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96143592T>C , CM000664.2:g.96143592T>C GRCh38
NC_000002.11:g.96809331T>C , CM000664.1:g.96809331T>C GRCh37
NC_000002.10:g.96173058T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000288943.5:c.*231A>G MANE Select ENSP00000288943.4:n.*231A>G
ENST00000288943.4:c.*231A>G ENSP00000288943.4:n.*231A>G
NM_004418.3:c.*231A>G NP_004409.1:n.*231A>G
XM_017003546.1:c.*231A>G XP_016859035.1:n.*231A>G
NM_004418.4:c.*231A>G MANE Select NP_004409.1:n.*231A>G
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