Canonical Allele Identifier: CA2669788685
Gene: MSX1 HGNC NCBI

Linked Data

gnomAD v4: 4-4863253-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4863253A>G , CM000666.2:g.4863253A>G GRCh38
NC_000004.11:g.4864980A>G , CM000666.1:g.4864980A>G GRCh37
NC_000004.10:g.4915881A>G NCBI36
NG_008121.1:g.8589A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.*110A>G MANE Select ENSP00000372170.4:n.*110A>G
ENST00000382723.4:c.*110A>G ENSP00000372170.4:n.*110A>G
NM_002448.3:c.*110A>G MANE Select NP_002439.2:n.*110A>G
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