Canonical Allele Identifier: CA438195521
Gene: MSX1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.4864837C>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4863110C>G , CM000666.2:g.4863110C>G GRCh38
NC_000004.11:g.4864837C>G , CM000666.1:g.4864837C>G GRCh37
NC_000004.10:g.4915738C>G NCBI36
NG_008121.1:g.8446C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.879C>G MANE Select ENSP00000372170.4:p.Ala293=
ENST00000382723.4:c.879C>G ENSP00000372170.4:p.Ala293=
NM_002448.3:c.879C>G MANE Select NP_002439.2:p.Ala293=
Search 100 bp 5'
Search 100 bp 3'