Canonical Allele Identifier: CA1229178630
Gene: GREM2 HGNC NCBI

Linked Data

dbSNP Id: rs1678621095
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.240542731T>A , CM000663.2:g.240542731T>A GRCh38
NC_000001.10:g.240706031T>A , CM000663.1:g.240706031T>A GRCh37
NC_000001.9:g.238772654T>A NCBI36
NG_053136.1:g.74642A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000318160.5:c.-1-49255A>T MANE Select ENSP00000318650.4:n.-1-49255A>T
ENST00000318160.4:c.-1-49255A>T ENSP00000318650.4:n.-1-49255A>T
NM_022469.3:c.-1-49255A>T NP_071914.3:n.-1-49255A>T
XM_011544249.1:c.-121-45134A>T XP_011542551.1:n.-121-45134A>T
XM_011544249.2:c.-121-45134A>T XP_011542551.1:n.-121-45134A>T
NM_022469.4:c.-1-49255A>T MANE Select NP_071914.3:n.-1-49255A>T
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