Canonical Allele Identifier: CA1013953592

Gene: GREM2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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