Canonical Allele Identifier: CA132700880
Gene: MSX2 HGNC NCBI

Linked Data

dbSNP Id: rs925070690

Genomic Alleles

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

Transcript Alleles

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