Canonical Allele Identifier: CA1229185203
Gene: GREM2 HGNC NCBI

Linked Data

dbSNP Id: rs1678985720

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.240558288T>C , CM000663.2:g.240558288T>C GRCh38
NC_000001.10:g.240721588T>C , CM000663.1:g.240721588T>C GRCh37
NC_000001.9:g.238788211T>C NCBI36
NG_053136.1:g.59085A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000318160.5:c.-2+53596A>G MANE Select ENSP00000318650.4:n.-2+53596A>G
ENST00000318160.4:c.-2+53596A>G ENSP00000318650.4:n.-2+53596A>G
NM_022469.3:c.-2+53596A>G NP_071914.3:n.-2+53596A>G
XM_011544249.1:c.-122+53596A>G XP_011542551.1:n.-122+53596A>G
XR_949319.1:n.219+2076T>C
XM_011544249.2:c.-122+53596A>G XP_011542551.1:n.-122+53596A>G
NM_022469.4:c.-2+53596A>G MANE Select NP_071914.3:n.-2+53596A>G