Canonical Allele Identifier: CA1602344881
Gene: MSX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724567G= , CM000667.2:g.174724567G= GRCh38
NC_000005.9:g.174151570G= , CM000667.1:g.174151570G= GRCh37
NC_000005.8:g.174084176G= NCBI36
NG_008124.1:g.4996G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.6:c.-93G= ENSP00000239243.5:n.-93G=