Canonical Allele Identifier: CA2509267494
Gene: GREM2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.240558278G>T , CM000663.2:g.240558278G>T GRCh38
NC_000001.10:g.240721578G>T , CM000663.1:g.240721578G>T GRCh37
NC_000001.9:g.238788201G>T NCBI36
NG_053136.1:g.59095C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000318160.5:c.-2+53606C>A MANE Select ENSP00000318650.4:n.-2+53606C>A
ENST00000318160.4:c.-2+53606C>A ENSP00000318650.4:n.-2+53606C>A
NM_022469.3:c.-2+53606C>A NP_071914.3:n.-2+53606C>A
XM_011544249.1:c.-122+53606C>A XP_011542551.1:n.-122+53606C>A
XR_949319.1:n.219+2066G>T
XM_011544249.2:c.-122+53606C>A XP_011542551.1:n.-122+53606C>A
NM_022469.4:c.-2+53606C>A MANE Select NP_071914.3:n.-2+53606C>A
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