Canonical Allele Identifier: CA1602344876
Gene: MSX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724566C= , CM000667.2:g.174724566C= GRCh38
NC_000005.9:g.174151569C= , CM000667.1:g.174151569C= GRCh37
NC_000005.8:g.174084175C= NCBI36
NG_008124.1:g.4995C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.6:c.-94C= ENSP00000239243.5:n.-94C=