Canonical Allele Identifier: CA733555595

Gene: GREM2

Linked Data

• dbSNP Id: rs1331571349
• MyVariant Identifiers: chr1:g.240705927T>C (hg19) ; chr1:g.240542627T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.240542627T>C , CM000663.2:g.240542627T>C	GRCh38
NC_000001.10:g.240705927T>C , CM000663.1:g.240705927T>C	GRCh37
NC_000001.9:g.238772550T>C	NCBI36
NG_053136.1:g.74746A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318160.5:c.-1-49151A>G MANE Select	ENSP00000318650.4:n.-1-49151A>G
ENST00000318160.4:c.-1-49151A>G	ENSP00000318650.4:n.-1-49151A>G
NM_022469.3:c.-1-49151A>G	NP_071914.3:n.-1-49151A>G
XM_011544249.1:c.-121-45030A>G	XP_011542551.1:n.-121-45030A>G
XM_011544249.2:c.-121-45030A>G	XP_011542551.1:n.-121-45030A>G
NM_022469.4:c.-1-49151A>G MANE Select	NP_071914.3:n.-1-49151A>G