Canonical Allele Identifier: CA2669788679
Gene: MSX1 HGNC NCBI

Linked Data

gnomAD v4: 4-4863250-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4863250C>G , CM000666.2:g.4863250C>G GRCh38
NC_000004.11:g.4864977C>G , CM000666.1:g.4864977C>G GRCh37
NC_000004.10:g.4915878C>G NCBI36
NG_008121.1:g.8586C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.*107C>G MANE Select ENSP00000372170.4:n.*107C>G
ENST00000382723.4:c.*107C>G ENSP00000372170.4:n.*107C>G
NM_002448.3:c.*107C>G MANE Select NP_002439.2:n.*107C>G
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