Canonical Allele Identifier: CA438365771
Gene: MSX1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.4861911A>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4860184A>G , CM000666.2:g.4860184A>G GRCh38
NC_000004.11:g.4861911A>G , CM000666.1:g.4861911A>G GRCh37
NC_000004.10:g.4912812A>G NCBI36
NG_008121.1:g.5520A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.285A>G MANE Select ENSP00000372170.4:p.Pro95=
ENST00000382723.4:c.285A>G ENSP00000372170.4:p.Pro95=
NM_002448.3:c.285A>G MANE Select NP_002439.2:p.Pro95=
Search 100 bp 5'
Search 100 bp 3'