Canonical Allele Identifier: CA2578488453
Gene: MSX2 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

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