Canonical Allele Identifier: CA2506276233
Gene: GREM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.240542745A>C , CM000663.2:g.240542745A>C GRCh38
NC_000001.10:g.240706045A>C , CM000663.1:g.240706045A>C GRCh37
NC_000001.9:g.238772668A>C NCBI36
NG_053136.1:g.74628T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000318160.5:c.-1-49269T>G MANE Select ENSP00000318650.4:n.-1-49269T>G
ENST00000318160.4:c.-1-49269T>G ENSP00000318650.4:n.-1-49269T>G
NM_022469.3:c.-1-49269T>G NP_071914.3:n.-1-49269T>G
XM_011544249.1:c.-121-45148T>G XP_011542551.1:n.-121-45148T>G
XM_011544249.2:c.-121-45148T>G XP_011542551.1:n.-121-45148T>G
NM_022469.4:c.-1-49269T>G MANE Select NP_071914.3:n.-1-49269T>G