Canonical Allele Identifier: CA2669788602
Gene: MSX1 HGNC NCBI

Linked Data

gnomAD v4: 4-4863170-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4863170C>A , CM000666.2:g.4863170C>A GRCh38
NC_000004.11:g.4864897C>A , CM000666.1:g.4864897C>A GRCh37
NC_000004.10:g.4915798C>A NCBI36
NG_008121.1:g.8506C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.*27C>A MANE Select ENSP00000372170.4:n.*27C>A
ENST00000382723.4:c.*27C>A ENSP00000372170.4:n.*27C>A
NM_002448.3:c.*27C>A MANE Select NP_002439.2:n.*27C>A
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