Canonical Allele Identifier: CA40346862
Gene: GREM2 HGNC NCBI

Linked Data

dbSNP Id: rs867924750
gnomAD v3: 1-240542785-T-C
gnomAD v4: 1-240542785-T-C
MyVariant Identifiers: chr1:g.240706085T>C (hg19) chr1:g.240542785T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.240542785T>C , CM000663.2:g.240542785T>C GRCh38
NC_000001.10:g.240706085T>C , CM000663.1:g.240706085T>C GRCh37
NC_000001.9:g.238772708T>C NCBI36
NG_053136.1:g.74588A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000318160.5:c.-1-49309A>G MANE Select ENSP00000318650.4:n.-1-49309A>G
ENST00000318160.4:c.-1-49309A>G ENSP00000318650.4:n.-1-49309A>G
NM_022469.3:c.-1-49309A>G NP_071914.3:n.-1-49309A>G
XM_011544249.1:c.-121-45188A>G XP_011542551.1:n.-121-45188A>G
XM_011544249.2:c.-121-45188A>G XP_011542551.1:n.-121-45188A>G
NM_022469.4:c.-1-49309A>G MANE Select NP_071914.3:n.-1-49309A>G
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