Canonical Allele Identifier: CA1160483503
Gene: WASF2 HGNC NCBI

Linked Data

dbSNP Id: rs1571112684
gnomAD v4: 1-27405061-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.27405061C>T , CM000663.2:g.27405061C>T GRCh38
NC_000001.10:g.27731565C>T , CM000663.1:g.27731565C>T GRCh37
NC_000001.9:g.27604152C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000618852.5:c.*3128G>A MANE Select ENSP00000483313.1:n.*3128G>A
ENST00000618852.4:c.*3128G>A ENSP00000483313.1:n.*3128G>A
NM_001201404.2:c.*3264G>A NP_001188333.1:n.*3264G>A
NM_006990.4:c.*3128G>A NP_008921.1:n.*3128G>A
NM_006990.5:c.*3128G>A MANE Select NP_008921.1:n.*3128G>A
NM_001201404.3:c.*3264G>A NP_001188333.1:n.*3264G>A
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