Canonical Allele Identifier: CA913410230
Gene: GREM2 HGNC NCBI

Linked Data

gnomAD v2: 1-240706046-TAAG-T
gnomAD v3: 1-240542746-TAAG-T
gnomAD v4: 1-240542746-TAAG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.240542751_240542753del , CM000663.2:g.240542751_240542753del GRCh38
NC_000001.10:g.240706051_240706053del , CM000663.1:g.240706051_240706053del GRCh37
NC_000001.9:g.238772674_238772676del NCBI36
NG_053136.1:g.74624_74626del

Transcript Alleles

HGVS Amino-acid change
ENST00000318160.5:c.-1-49273_-1-49271del MANE Select ENSP00000318650.4:n.-1-49273_-1-49271del
ENST00000318160.4:c.-1-49273_-1-49271del ENSP00000318650.4:n.-1-49273_-1-49271del
NM_022469.3:c.-1-49273_-1-49271del NP_071914.3:n.-1-49273_-1-49271del
XM_011544249.1:c.-121-45152_-121-45150del XP_011542551.1:n.-121-45152_-121-45150del...
XM_011544249.2:c.-121-45152_-121-45150del XP_011542551.1:n.-121-45152_-121-45150del...
NM_022469.4:c.-1-49273_-1-49271del MANE Select NP_071914.3:n.-1-49273_-1-49271del
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