Canonical Allele Identifier: CA1602344935
Gene: MSX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724580C= , CM000667.2:g.174724580C= GRCh38
NC_000005.9:g.174151583C= , CM000667.1:g.174151583C= GRCh37
NC_000005.8:g.174084189C= NCBI36
NG_008124.1:g.5009C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.6:c.-80C= ENSP00000239243.5:n.-80C=
NM_002449.4:c.-80C= NP_002440.2:n.-80C=
NM_001363626.1:c.-80C= NP_001350555.1:n.-80C=