Canonical Allele Identifier: CA733555666
Gene: GREM2 HGNC NCBI

Linked Data

dbSNP Id: rs1237776779
gnomAD v3: 1-240542776-A-G
gnomAD v4: 1-240542776-A-G
MyVariant Identifiers: chr1:g.240706076A>G (hg19) chr1:g.240542776A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.240542776A>G , CM000663.2:g.240542776A>G GRCh38
NC_000001.10:g.240706076A>G , CM000663.1:g.240706076A>G GRCh37
NC_000001.9:g.238772699A>G NCBI36
NG_053136.1:g.74597T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000318160.5:c.-1-49300T>C MANE Select ENSP00000318650.4:n.-1-49300T>C
ENST00000318160.4:c.-1-49300T>C ENSP00000318650.4:n.-1-49300T>C
NM_022469.3:c.-1-49300T>C NP_071914.3:n.-1-49300T>C
XM_011544249.1:c.-121-45179T>C XP_011542551.1:n.-121-45179T>C
XM_011544249.2:c.-121-45179T>C XP_011542551.1:n.-121-45179T>C
NM_022469.4:c.-1-49300T>C MANE Select NP_071914.3:n.-1-49300T>C
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