Canonical Allele Identifier: CA2676572655
Gene: MSX2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724578C>T , CM000667.2:g.174724578C>T GRCh38
NC_000005.9:g.174151581C>T , CM000667.1:g.174151581C>T GRCh37
NC_000005.8:g.174084187C>T NCBI36
NG_008124.1:g.5007C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.6:c.-82C>T ENSP00000239243.5:n.-82C>T
NM_002449.4:c.-82C>T NP_002440.2:n.-82C>T
NM_001363626.1:c.-82C>T NP_001350555.1:n.-82C>T