Canonical Allele Identifier: CA2669788138
Gene: MSX1 HGNC NCBI

Linked Data

gnomAD v4: 4-4862316-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4862316A>G , CM000666.2:g.4862316A>G GRCh38
NC_000004.11:g.4864043A>G , CM000666.1:g.4864043A>G GRCh37
NC_000004.10:g.4914944A>G NCBI36
NG_008121.1:g.7652A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.470-385A>G MANE Select ENSP00000372170.4:n.470-385A>G
ENST00000382723.4:c.470-385A>G ENSP00000372170.4:n.470-385A>G
NM_002448.3:c.470-385A>G MANE Select NP_002439.2:n.470-385A>G
Search 100 bp 5'
Search 100 bp 3'