Canonical Allele Identifier: CA1602344897
Gene: MSX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724572T= , CM000667.2:g.174724572T= GRCh38
NC_000005.9:g.174151575T= , CM000667.1:g.174151575T= GRCh37
NC_000005.8:g.174084181T= NCBI36
NG_008124.1:g.5001T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.6:c.-88T= ENSP00000239243.5:n.-88T=
NM_002449.4:c.-88T= NP_002440.2:n.-88T=
NM_001363626.1:c.-88T= NP_001350555.1:n.-88T=