Canonical Allele Identifier: CA1602344901
Gene: MSX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724573C= , CM000667.2:g.174724573C= GRCh38
NC_000005.9:g.174151576C= , CM000667.1:g.174151576C= GRCh37
NC_000005.8:g.174084182C= NCBI36
NG_008124.1:g.5002C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.6:c.-87C= ENSP00000239243.5:n.-87C=
NM_002449.4:c.-87C= NP_002440.2:n.-87C=
NM_001363626.1:c.-87C= NP_001350555.1:n.-87C=