Canonical Allele Identifier: CA40346905
Gene: GREM2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10495471

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.240542807A>G , CM000663.2:g.240542807A>G GRCh38
NC_000001.9:g.238772730A>G NCBI36
NC_000001.10:g.240706107A>G , CM000663.1:g.240706107A>G GRCh37

Transcript Alleles

HGVS Amino-acid change
ENST00000318160.4:c.-1-49331T>C ENSP00000318650.4:p.=
NM_022469.3:c.-1-49331T>C VV NP_071914.3:p.=
XM_011544249.1:c.-121-45210T>C XP_011542551.1:p.=