Canonical Allele Identifier: CA1229185190
Gene: GREM2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.240558267A= , CM000663.2:g.240558267A= GRCh38
NC_000001.10:g.240721567A= , CM000663.1:g.240721567A= GRCh37
NC_000001.9:g.238788190A= NCBI36
NG_053136.1:g.59106T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000318160.5:c.-2+53617T= MANE Select ENSP00000318650.4:n.-2+53617T=
ENST00000318160.4:c.-2+53617T= ENSP00000318650.4:n.-2+53617T=
NM_022469.3:c.-2+53617T= NP_071914.3:n.-2+53617T=
XM_011544249.1:c.-122+53617T= XP_011542551.1:n.-122+53617T=
XR_949319.1:n.219+2055A=
XM_011544249.2:c.-122+53617T= XP_011542551.1:n.-122+53617T=
NM_022469.4:c.-2+53617T= MANE Select NP_071914.3:n.-2+53617T=
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