Canonical Allele Identifier: CA356139161
Gene: MSX1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.4864823G>A (hg19) chr4:g.4863096G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4863096G>A , CM000666.2:g.4863096G>A GRCh38
NC_000004.11:g.4864823G>A , CM000666.1:g.4864823G>A GRCh37
NC_000004.10:g.4915724G>A NCBI36
NG_008121.1:g.8432G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.865G>A MANE Select ENSP00000372170.4:p.Gly289Arg
ENST00000382723.4:c.865G>A ENSP00000372170.4:p.Gly289Arg
NM_002448.3:c.865G>A MANE Select NP_002439.2:p.Gly289Arg
Search 100 bp 5'
Search 100 bp 3'