Canonical Allele Identifier: CA356137791
Gene: MSX1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.4861966C>A (hg19) chr4:g.4860239C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4860239C>A , CM000666.2:g.4860239C>A GRCh38
NC_000004.11:g.4861966C>A , CM000666.1:g.4861966C>A GRCh37
NC_000004.10:g.4912867C>A NCBI36
NG_008121.1:g.5575C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000382723.5:c.340C>A MANE Select ENSP00000372170.4:p.Pro114Thr
ENST00000382723.4:c.340C>A ENSP00000372170.4:p.Pro114Thr
NM_002448.3:c.340C>A MANE Select NP_002439.2:p.Pro114Thr
Search 100 bp 5'
Search 100 bp 3'