Canonical Allele Identifier: CA362229511
Gene: MSX2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724955T>C , CM000667.2:g.174724955T>C GRCh38
NC_000005.9:g.174151958T>C , CM000667.1:g.174151958T>C GRCh37
NC_000005.8:g.174084564T>C NCBI36
NG_008124.1:g.5384T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.7:c.296T>C MANE Select ENSP00000239243.5:p.Phe99Ser
ENST00000239243.6:c.296T>C ENSP00000239243.5:p.Phe99Ser
ENST00000507785.2:c.296T>C ENSP00000427425.1:p.Phe99Ser
NM_002449.4:c.296T>C NP_002440.2:p.Phe99Ser
NM_001363626.1:c.296T>C NP_001350555.1:p.Phe99Ser
NM_002449.5:c.296T>C MANE Select NP_002440.2:p.Phe99Ser
NM_001363626.2:c.296T>C NP_001350555.1:p.Phe99Ser