Canonical Allele Identifier: CA438366382
Gene: MSX1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.4864762T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4863035T>A , CM000666.2:g.4863035T>A GRCh38
NC_000004.11:g.4864762T>A , CM000666.1:g.4864762T>A GRCh37
NC_000004.10:g.4915663T>A NCBI36
NG_008121.1:g.8371T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.804T>A MANE Select ENSP00000372170.4:p.Gly268=
ENST00000382723.4:c.804T>A ENSP00000372170.4:p.Gly268=
NM_002448.3:c.804T>A MANE Select NP_002439.2:p.Gly268=
Search 100 bp 5'
Search 100 bp 3'