Canonical Allele Identifier: CA733555641
Gene: GREM2 HGNC NCBI

Linked Data

dbSNP Id: rs1220388180
gnomAD v3: 1-240542739-T-C
gnomAD v4: 1-240542739-T-C
MyVariant Identifiers: chr1:g.240706039T>C (hg19) chr1:g.240542739T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.240542739T>C , CM000663.2:g.240542739T>C GRCh38
NC_000001.10:g.240706039T>C , CM000663.1:g.240706039T>C GRCh37
NC_000001.9:g.238772662T>C NCBI36
NG_053136.1:g.74634A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000318160.5:c.-1-49263A>G MANE Select ENSP00000318650.4:n.-1-49263A>G
ENST00000318160.4:c.-1-49263A>G ENSP00000318650.4:n.-1-49263A>G
NM_022469.3:c.-1-49263A>G NP_071914.3:n.-1-49263A>G
XM_011544249.1:c.-121-45142A>G XP_011542551.1:n.-121-45142A>G
XM_011544249.2:c.-121-45142A>G XP_011542551.1:n.-121-45142A>G
NM_022469.4:c.-1-49263A>G MANE Select NP_071914.3:n.-1-49263A>G
Search 100 bp 5'
Search 100 bp 3'