Canonical Allele Identifier: CA11075636

Gene: DUSP2

Linked Data

• dbSNP Id: rs1724120
• gnomAD v2: 2-96809331-T-C
• gnomAD v3: 2-96143592-T-C
• gnomAD v4: 2-96143592-T-C
• MyVariant Identifiers: chr2:g.96809331T>C (hg19) ; chr2:g.96143592T>C (hg38)

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