Canonical Allele Identifier: CA1435013587
Gene: MSX1 HGNC NCBI

Linked Data

dbSNP Id: rs1737944355
gnomAD v4: 4-4862675-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4862675T>C , CM000666.2:g.4862675T>C GRCh38
NC_000004.11:g.4864402T>C , CM000666.1:g.4864402T>C GRCh37
NC_000004.10:g.4915303T>C NCBI36
NG_008121.1:g.8011T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000382723.5:c.470-26T>C MANE Select ENSP00000372170.4:n.470-26T>C
ENST00000382723.4:c.470-26T>C ENSP00000372170.4:n.470-26T>C
ENST00000468421.1:n.182-26T>C
NM_002448.3:c.470-26T>C MANE Select NP_002439.2:n.470-26T>C
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