Canonical Allele Identifier: CA362229141
Gene: MSX2 HGNC NCBI

Linked Data

dbSNP Id: rs1760739692

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724771C>G , CM000667.2:g.174724771C>G GRCh38
NC_000005.9:g.174151774C>G , CM000667.1:g.174151774C>G GRCh37
NC_000005.8:g.174084380C>G NCBI36
NG_008124.1:g.5200C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.7:c.112C>G MANE Select ENSP00000239243.5:p.Arg38Gly
ENST00000239243.6:c.112C>G ENSP00000239243.5:p.Arg38Gly
ENST00000507785.2:c.112C>G ENSP00000427425.1:p.Arg38Gly
NM_002449.4:c.112C>G NP_002440.2:p.Arg38Gly
NM_001363626.1:c.112C>G NP_001350555.1:p.Arg38Gly
NM_002449.5:c.112C>G MANE Select NP_002440.2:p.Arg38Gly
NM_001363626.2:c.112C>G NP_001350555.1:p.Arg38Gly