Canonical Allele Identifier: CA1141960566
Gene: GREM2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.240558266G= , CM000663.2:g.240558266G= GRCh38
NC_000001.10:g.240721566G= , CM000663.1:g.240721566G= GRCh37
NC_000001.9:g.238788189G= NCBI36
NG_053136.1:g.59107C=

Transcript Alleles

HGVS Amino-acid change
ENST00000318160.5:c.-2+53618C= MANE Select ENSP00000318650.4:n.-2+53618C=
ENST00000318160.4:c.-2+53618C= ENSP00000318650.4:n.-2+53618C=
NM_022469.3:c.-2+53618C= NP_071914.3:n.-2+53618C=
XM_011544249.1:c.-122+53618C= XP_011542551.1:n.-122+53618C=
XR_949319.1:n.219+2054G=
XM_011544249.2:c.-122+53618C= XP_011542551.1:n.-122+53618C=
NM_022469.4:c.-2+53618C= MANE Select NP_071914.3:n.-2+53618C=
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