Canonical Allele Identifier: CA1602344887
Gene: MSX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724569C= , CM000667.2:g.174724569C= GRCh38
NC_000005.9:g.174151572C= , CM000667.1:g.174151572C= GRCh37
NC_000005.8:g.174084178C= NCBI36
NG_008124.1:g.4998C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.6:c.-91C= ENSP00000239243.5:n.-91C=