Canonical Allele Identifier: CA438195519
Gene: MSX1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.4864834G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4863107G>T , CM000666.2:g.4863107G>T GRCh38
NC_000004.11:g.4864834G>T , CM000666.1:g.4864834G>T GRCh37
NC_000004.10:g.4915735G>T NCBI36
NG_008121.1:g.8443G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.876G>T MANE Select ENSP00000372170.4:p.Thr292=
ENST00000382723.4:c.876G>T ENSP00000372170.4:p.Thr292=
NM_002448.3:c.876G>T MANE Select NP_002439.2:p.Thr292=
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