Canonical Allele Identifier: CA438365533
Gene: MSX1 HGNC NCBI

Linked Data

gnomAD v4: 4-4860352-C-T
MyVariant Identifiers: chr4:g.4862079C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4860352C>T , CM000666.2:g.4860352C>T GRCh38
NC_000004.11:g.4862079C>T , CM000666.1:g.4862079C>T GRCh37
NC_000004.10:g.4912980C>T NCBI36
NG_008121.1:g.5688C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.453C>T MANE Select ENSP00000372170.4:p.Phe151=
ENST00000382723.4:c.453C>T ENSP00000372170.4:p.Phe151=
NM_002448.3:c.453C>T MANE Select NP_002439.2:p.Phe151=
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