Canonical Allele Identifier: CA534360276

Gene: DUSP2

Linked Data

• dbSNP Id: rs1202381934
• gnomAD v2: 2-96809128-C-A
• gnomAD v3: 2-96143389-C-A
• gnomAD v4: 2-96143389-C-A
• MyVariant Identifiers: chr2:g.96809128C>A (hg19) ; chr2:g.96143389C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96143389C>A , CM000664.2:g.96143389C>A	GRCh38
NC_000002.11:g.96809128C>A , CM000664.1:g.96809128C>A	GRCh37
NC_000002.10:g.96172855C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288943.5:c.*434G>T MANE Select	ENSP00000288943.4:n.*434G>T
ENST00000288943.4:c.*434G>T	ENSP00000288943.4:n.*434G>T
NM_004418.3:c.*434G>T	NP_004409.1:n.*434G>T
XM_017003546.1:c.*434G>T	XP_016859035.1:n.*434G>T
NM_004418.4:c.*434G>T MANE Select	NP_004409.1:n.*434G>T