Canonical Allele Identifier: CA438365858
Gene: MSX1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.4861983G>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4860256G>A , CM000666.2:g.4860256G>A GRCh38
NC_000004.11:g.4861983G>A , CM000666.1:g.4861983G>A GRCh37
NC_000004.10:g.4912884G>A NCBI36
NG_008121.1:g.5592G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.357G>A MANE Select ENSP00000372170.4:p.Ser119=
ENST00000382723.4:c.357G>A ENSP00000372170.4:p.Ser119=
NM_002448.3:c.357G>A MANE Select NP_002439.2:p.Ser119=
Search 100 bp 5'
Search 100 bp 3'