Canonical Allele Identifier: CA2676572643
Gene: MSX2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724563G>C , CM000667.2:g.174724563G>C GRCh38
NC_000005.9:g.174151566G>C , CM000667.1:g.174151566G>C GRCh37
NC_000005.8:g.174084172G>C NCBI36
NG_008124.1:g.4992G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.6:c.-97G>C ENSP00000239243.5:n.-97G>C