Canonical Allele Identifier: CA3565147
Gene: MSX2 HGNC NCBI

Linked Data

dbSNP Id: rs771889290

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174725021G>A , CM000667.2:g.174725021G>A GRCh38
NC_000005.9:g.174152024G>A , CM000667.1:g.174152024G>A GRCh37
NC_000005.8:g.174084630G>A NCBI36
NG_008124.1:g.5450G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.7:c.362G>A MANE Select ENSP00000239243.5:p.Arg121Gln
ENST00000239243.6:c.362G>A ENSP00000239243.5:p.Arg121Gln
ENST00000507785.2:c.362G>A ENSP00000427425.1:p.Arg121Gln
NM_002449.4:c.362G>A NP_002440.2:p.Arg121Gln
NM_001363626.1:c.362G>A NP_001350555.1:p.Arg121Gln
NM_002449.5:c.362G>A MANE Select NP_002440.2:p.Arg121Gln
NM_001363626.2:c.362G>A NP_001350555.1:p.Arg121Gln