Canonical Allele Identifier: CA1435013353
Gene: MSX1 HGNC NCBI

Linked Data

dbSNP Id: rs1328211387
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4862261C>G , CM000666.2:g.4862261C>G GRCh38
NC_000004.11:g.4863988C>G , CM000666.1:g.4863988C>G GRCh37
NC_000004.10:g.4914889C>G NCBI36
NG_008121.1:g.7597C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.470-440C>G MANE Select ENSP00000372170.4:n.470-440C>G
ENST00000382723.4:c.470-440C>G ENSP00000372170.4:n.470-440C>G
NM_002448.3:c.470-440C>G MANE Select NP_002439.2:n.470-440C>G
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