Canonical Allele Identifier: CA1602344869
Gene: MSX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724564C= , CM000667.2:g.174724564C= GRCh38
NC_000005.9:g.174151567C= , CM000667.1:g.174151567C= GRCh37
NC_000005.8:g.174084173C= NCBI36
NG_008124.1:g.4993C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.6:c.-96C= ENSP00000239243.5:n.-96C=