Canonical Allele Identifier: CA1013953587

Gene: GREM2

Linked Data

• dbSNP Id: rs1678985347
• gnomAD v3: 1-240558273-T-C
• gnomAD v4: 1-240558273-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.240558273T>C , CM000663.2:g.240558273T>C	GRCh38
NC_000001.10:g.240721573T>C , CM000663.1:g.240721573T>C	GRCh37
NC_000001.9:g.238788196T>C	NCBI36
NG_053136.1:g.59100A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318160.5:c.-2+53611A>G MANE Select	ENSP00000318650.4:n.-2+53611A>G
ENST00000318160.4:c.-2+53611A>G	ENSP00000318650.4:n.-2+53611A>G
NM_022469.3:c.-2+53611A>G	NP_071914.3:n.-2+53611A>G
XM_011544249.1:c.-122+53611A>G	XP_011542551.1:n.-122+53611A>G
XR_949319.1:n.219+2061T>C
XM_011544249.2:c.-122+53611A>G	XP_011542551.1:n.-122+53611A>G
NM_022469.4:c.-2+53611A>G MANE Select	NP_071914.3:n.-2+53611A>G