Canonical Allele Identifier: CA2669788692
Gene: MSX1 HGNC NCBI

Linked Data

gnomAD v4: 4-4863260-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4863260T>C , CM000666.2:g.4863260T>C GRCh38
NC_000004.11:g.4864987T>C , CM000666.1:g.4864987T>C GRCh37
NC_000004.10:g.4915888T>C NCBI36
NG_008121.1:g.8596T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.*117T>C MANE Select ENSP00000372170.4:n.*117T>C
ENST00000382723.4:c.*117T>C ENSP00000372170.4:n.*117T>C
NM_002448.3:c.*117T>C MANE Select NP_002439.2:n.*117T>C
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