Canonical Allele Identifier: CA40346806
Gene: GREM2 HGNC NCBI

Linked Data

dbSNP Id: rs765560514
gnomAD v3: 1-240542677-G-T
gnomAD v4: 1-240542677-G-T
COSMIC: COSN8451355
MyVariant Identifiers: chr1:g.240705977G>T (hg19) chr1:g.240542677G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.240542677G>T , CM000663.2:g.240542677G>T GRCh38
NC_000001.10:g.240705977G>T , CM000663.1:g.240705977G>T GRCh37
NC_000001.9:g.238772600G>T NCBI36
NG_053136.1:g.74696C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000318160.5:c.-1-49201C>A MANE Select ENSP00000318650.4:n.-1-49201C>A
ENST00000318160.4:c.-1-49201C>A ENSP00000318650.4:n.-1-49201C>A
NM_022469.3:c.-1-49201C>A NP_071914.3:n.-1-49201C>A
XM_011544249.1:c.-121-45080C>A XP_011542551.1:n.-121-45080C>A
XM_011544249.2:c.-121-45080C>A XP_011542551.1:n.-121-45080C>A
NM_022469.4:c.-1-49201C>A MANE Select NP_071914.3:n.-1-49201C>A
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