Canonical Allele Identifier: CA1013953594

Gene: GREM2

Linked Data

• dbSNP Id: rs1678985425
• gnomAD v3: 1-240558277-A-T
• gnomAD v4: 1-240558277-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.240558277A>T , CM000663.2:g.240558277A>T	GRCh38
NC_000001.10:g.240721577A>T , CM000663.1:g.240721577A>T	GRCh37
NC_000001.9:g.238788200A>T	NCBI36
NG_053136.1:g.59096T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318160.5:c.-2+53607T>A MANE Select	ENSP00000318650.4:n.-2+53607T>A
ENST00000318160.4:c.-2+53607T>A	ENSP00000318650.4:n.-2+53607T>A
NM_022469.3:c.-2+53607T>A	NP_071914.3:n.-2+53607T>A
XM_011544249.1:c.-122+53607T>A	XP_011542551.1:n.-122+53607T>A
XR_949319.1:n.219+2065A>T
XM_011544249.2:c.-122+53607T>A	XP_011542551.1:n.-122+53607T>A
NM_022469.4:c.-2+53607T>A MANE Select	NP_071914.3:n.-2+53607T>A