Canonical Allele Identifier: CA1602344971
Gene: MSX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724588A= , CM000667.2:g.174724588A= GRCh38
NC_000005.9:g.174151591A= , CM000667.1:g.174151591A= GRCh37
NC_000005.8:g.174084197A= NCBI36
NG_008124.1:g.5017A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.7:c.-72A= MANE Select ENSP00000239243.5:n.-72A=
ENST00000239243.6:c.-72A= ENSP00000239243.5:n.-72A=
NM_002449.4:c.-72A= NP_002440.2:n.-72A=
NM_001363626.1:c.-72A= NP_001350555.1:n.-72A=
NM_002449.5:c.-72A= MANE Select NP_002440.2:n.-72A=
NM_001363626.2:c.-72A= NP_001350555.1:n.-72A=