Canonical Allele Identifier: CA91672560
Gene: MSX1 HGNC NCBI

Linked Data

dbSNP Id: rs1053947732
gnomAD v4: 4-4863175-C-T
MyVariant Identifiers: chr4:g.4863175C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4863175C>T , CM000666.2:g.4863175C>T GRCh38
NC_000004.11:g.4864902C>T , CM000666.1:g.4864902C>T GRCh37
NC_000004.10:g.4915803C>T NCBI36
NG_008121.1:g.8511C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.*32C>T MANE Select ENSP00000372170.4:n.*32C>T
ENST00000382723.4:c.*32C>T ENSP00000372170.4:n.*32C>T
NM_002448.3:c.*32C>T MANE Select NP_002439.2:n.*32C>T
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