Canonical Allele Identifier: CA2676572654
Gene: MSX2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724576G>T , CM000667.2:g.174724576G>T GRCh38
NC_000005.9:g.174151579G>T , CM000667.1:g.174151579G>T GRCh37
NC_000005.8:g.174084185G>T NCBI36
NG_008124.1:g.5005G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.6:c.-84G>T ENSP00000239243.5:n.-84G>T
NM_002449.4:c.-84G>T NP_002440.2:n.-84G>T
NM_001363626.1:c.-84G>T NP_001350555.1:n.-84G>T