Canonical Allele Identifier: CA1602346340
Gene: MSX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724930A= , CM000667.2:g.174724930A= GRCh38
NC_000005.9:g.174151933A= , CM000667.1:g.174151933A= GRCh37
NC_000005.8:g.174084539A= NCBI36
NG_008124.1:g.5359A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.7:c.271A= MANE Select ENSP00000239243.5:p.Ser91=
ENST00000239243.6:c.271A= ENSP00000239243.5:p.Ser91=
ENST00000507785.2:c.271A= ENSP00000427425.1:p.Ser91=
NM_002449.4:c.271A= NP_002440.2:p.Ser91=
NM_001363626.1:c.271A= NP_001350555.1:p.Ser91=
NM_002449.5:c.271A= MANE Select NP_002440.2:p.Ser91=
NM_001363626.2:c.271A= NP_001350555.1:p.Ser91=