Canonical Allele Identifier: CA40346855

Gene: GREM2

Linked Data

• dbSNP Id: rs962300533
• MyVariant Identifiers: chr1:g.240706073G>A (hg19) ; chr1:g.240542773G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.240542773G>A , CM000663.2:g.240542773G>A	GRCh38
NC_000001.10:g.240706073G>A , CM000663.1:g.240706073G>A	GRCh37
NC_000001.9:g.238772696G>A	NCBI36
NG_053136.1:g.74600C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000318160.5:c.-1-49297C>T MANE Select	ENSP00000318650.4:n.-1-49297C>T
ENST00000318160.4:c.-1-49297C>T	ENSP00000318650.4:n.-1-49297C>T
NM_022469.3:c.-1-49297C>T	NP_071914.3:n.-1-49297C>T
XM_011544249.1:c.-121-45176C>T	XP_011542551.1:n.-121-45176C>T
XM_011544249.2:c.-121-45176C>T	XP_011542551.1:n.-121-45176C>T
NM_022469.4:c.-1-49297C>T MANE Select	NP_071914.3:n.-1-49297C>T