Canonical Allele Identifier: CA2669788106
Gene: MSX1 HGNC NCBI

Linked Data

gnomAD v4: 4-4862292-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4862292T>A , CM000666.2:g.4862292T>A GRCh38
NC_000004.11:g.4864019T>A , CM000666.1:g.4864019T>A GRCh37
NC_000004.10:g.4914920T>A NCBI36
NG_008121.1:g.7628T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.470-409T>A MANE Select ENSP00000372170.4:n.470-409T>A
ENST00000382723.4:c.470-409T>A ENSP00000372170.4:n.470-409T>A
NM_002448.3:c.470-409T>A MANE Select NP_002439.2:n.470-409T>A
Search 100 bp 5'
Search 100 bp 3'