Canonical Allele Identifier: CA2669788113
Gene: MSX1 HGNC NCBI

Linked Data

gnomAD v4: 4-4862296-T-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4862296T>G , CM000666.2:g.4862296T>G GRCh38
NC_000004.11:g.4864023T>G , CM000666.1:g.4864023T>G GRCh37
NC_000004.10:g.4914924T>G NCBI36
NG_008121.1:g.7632T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.470-405T>G MANE Select ENSP00000372170.4:n.470-405T>G
ENST00000382723.4:c.470-405T>G ENSP00000372170.4:n.470-405T>G
NM_002448.3:c.470-405T>G MANE Select NP_002439.2:n.470-405T>G
Search 100 bp 5'
Search 100 bp 3'