Canonical Allele Identifier: CA1435013390
Gene: MSX1 HGNC NCBI

Linked Data

dbSNP Id: rs1737934980
gnomAD v4: 4-4862343-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4862343C>T , CM000666.2:g.4862343C>T GRCh38
NC_000004.11:g.4864070C>T , CM000666.1:g.4864070C>T GRCh37
NC_000004.10:g.4914971C>T NCBI36
NG_008121.1:g.7679C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.470-358C>T MANE Select ENSP00000372170.4:n.470-358C>T
ENST00000382723.4:c.470-358C>T ENSP00000372170.4:n.470-358C>T
NM_002448.3:c.470-358C>T MANE Select NP_002439.2:n.470-358C>T
Search 100 bp 5'
Search 100 bp 3'