Canonical Allele Identifier: CA356138364
Gene: MSX1 HGNC NCBI

Linked Data

dbSNP Id: rs1737947693

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4862793G>C , CM000666.2:g.4862793G>C GRCh38
NC_000004.11:g.4864520G>C , CM000666.1:g.4864520G>C GRCh37
NC_000004.10:g.4915421G>C NCBI36
NG_008121.1:g.8129G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.562G>C MANE Select ENSP00000372170.4:p.Glu188Gln
ENST00000382723.4:c.562G>C ENSP00000372170.4:p.Glu188Gln
ENST00000468421.1:n.274G>C
NM_002448.3:c.562G>C MANE Select NP_002439.2:p.Glu188Gln