Canonical Allele Identifier: CA40346854
Gene: GREM2 HGNC NCBI

Linked Data

dbSNP Id: rs1015564600
MyVariant Identifiers: chr1:g.240706062C>T (hg19) chr1:g.240542762C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.240542762C>T , CM000663.2:g.240542762C>T GRCh38
NC_000001.10:g.240706062C>T , CM000663.1:g.240706062C>T GRCh37
NC_000001.9:g.238772685C>T NCBI36
NG_053136.1:g.74611G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000318160.5:c.-1-49286G>A MANE Select ENSP00000318650.4:n.-1-49286G>A
ENST00000318160.4:c.-1-49286G>A ENSP00000318650.4:n.-1-49286G>A
NM_022469.3:c.-1-49286G>A NP_071914.3:n.-1-49286G>A
XM_011544249.1:c.-121-45165G>A XP_011542551.1:n.-121-45165G>A
XM_011544249.2:c.-121-45165G>A XP_011542551.1:n.-121-45165G>A
NM_022469.4:c.-1-49286G>A MANE Select NP_071914.3:n.-1-49286G>A
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