Canonical Allele Identifier: CA40346757
Gene: GREM2 HGNC NCBI

Linked Data

dbSNP Id: rs572014984
gnomAD v3: 1-240542638-A-T
gnomAD v4: 1-240542638-A-T
MyVariant Identifiers: chr1:g.240705938A>T (hg19) chr1:g.240542638A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.240542638A>T , CM000663.2:g.240542638A>T GRCh38
NC_000001.10:g.240705938A>T , CM000663.1:g.240705938A>T GRCh37
NC_000001.9:g.238772561A>T NCBI36
NG_053136.1:g.74735T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000318160.5:c.-1-49162T>A MANE Select ENSP00000318650.4:n.-1-49162T>A
ENST00000318160.4:c.-1-49162T>A ENSP00000318650.4:n.-1-49162T>A
NM_022469.3:c.-1-49162T>A NP_071914.3:n.-1-49162T>A
XM_011544249.1:c.-121-45041T>A XP_011542551.1:n.-121-45041T>A
XM_011544249.2:c.-121-45041T>A XP_011542551.1:n.-121-45041T>A
NM_022469.4:c.-1-49162T>A MANE Select NP_071914.3:n.-1-49162T>A
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