Canonical Allele Identifier: CA1435013530
Gene: MSX1 HGNC NCBI

Linked Data

dbSNP Id: rs1193640475
gnomAD v4: 4-4862601-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4862601A>G , CM000666.2:g.4862601A>G GRCh38
NC_000004.11:g.4864328A>G , CM000666.1:g.4864328A>G GRCh37
NC_000004.10:g.4915229A>G NCBI36
NG_008121.1:g.7937A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.470-100A>G MANE Select ENSP00000372170.4:n.470-100A>G
ENST00000382723.4:c.470-100A>G ENSP00000372170.4:n.470-100A>G
ENST00000468421.1:n.174A>G
NM_002448.3:c.470-100A>G MANE Select NP_002439.2:n.470-100A>G
Search 100 bp 5'
Search 100 bp 3'