Canonical Allele Identifier: CA40346856
Gene: GREM2 HGNC NCBI

Linked Data

dbSNP Id: rs973677838
MyVariant Identifiers: chr1:g.240706082C>T (hg19) chr1:g.240542782C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.240542782C>T , CM000663.2:g.240542782C>T GRCh38
NC_000001.10:g.240706082C>T , CM000663.1:g.240706082C>T GRCh37
NC_000001.9:g.238772705C>T NCBI36
NG_053136.1:g.74591G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000318160.5:c.-1-49306G>A MANE Select ENSP00000318650.4:n.-1-49306G>A
ENST00000318160.4:c.-1-49306G>A ENSP00000318650.4:n.-1-49306G>A
NM_022469.3:c.-1-49306G>A NP_071914.3:n.-1-49306G>A
XM_011544249.1:c.-121-45185G>A XP_011542551.1:n.-121-45185G>A
XM_011544249.2:c.-121-45185G>A XP_011542551.1:n.-121-45185G>A
NM_022469.4:c.-1-49306G>A MANE Select NP_071914.3:n.-1-49306G>A
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