Canonical Allele Identifier: CA1602346254
Gene: MSX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724914C= , CM000667.2:g.174724914C= GRCh38
NC_000005.9:g.174151917C= , CM000667.1:g.174151917C= GRCh37
NC_000005.8:g.174084523C= NCBI36
NG_008124.1:g.5343C=

Transcript Alleles

HGVS Amino-acid change
ENST00000239243.7:c.255C= MANE Select ENSP00000239243.5:p.Gly85=
ENST00000239243.6:c.255C= ENSP00000239243.5:p.Gly85=
ENST00000507785.2:c.255C= ENSP00000427425.1:p.Gly85=
NM_002449.4:c.255C= NP_002440.2:p.Gly85=
NM_001363626.1:c.255C= NP_001350555.1:p.Gly85=
NM_002449.5:c.255C= MANE Select NP_002440.2:p.Gly85=
NM_001363626.2:c.255C= NP_001350555.1:p.Gly85=