Canonical Allele Identifier: CA1602345031
Gene: MSX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724600T= , CM000667.2:g.174724600T= GRCh38
NC_000005.9:g.174151603T= , CM000667.1:g.174151603T= GRCh37
NC_000005.8:g.174084209T= NCBI36
NG_008124.1:g.5029T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.7:c.-60T= MANE Select ENSP00000239243.5:n.-60T=
ENST00000239243.6:c.-60T= ENSP00000239243.5:n.-60T=
NM_002449.4:c.-60T= NP_002440.2:n.-60T=
NM_001363626.1:c.-60T= NP_001350555.1:n.-60T=
NM_002449.5:c.-60T= MANE Select NP_002440.2:n.-60T=
NM_001363626.2:c.-60T= NP_001350555.1:n.-60T=