Canonical Allele Identifier: CA2676572642
Gene: MSX2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724562A>T , CM000667.2:g.174724562A>T GRCh38
NC_000005.9:g.174151565A>T , CM000667.1:g.174151565A>T GRCh37
NC_000005.8:g.174084171A>T NCBI36
NG_008124.1:g.4991A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.6:c.-98A>T ENSP00000239243.5:n.-98A>T