Canonical Allele Identifier: CA91672598
Gene: MSX1 HGNC NCBI

Linked Data

dbSNP Id: rs137940514
gnomAD v2: 4-4864931-C-T
gnomAD v3: 4-4863204-C-T
gnomAD v4: 4-4863204-C-T
MyVariant Identifiers: chr4:g.4864931C>T (hg19) chr4:g.4863204C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4863204C>T , CM000666.2:g.4863204C>T GRCh38
NC_000004.11:g.4864931C>T , CM000666.1:g.4864931C>T GRCh37
NC_000004.10:g.4915832C>T NCBI36
NG_008121.1:g.8540C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.*61C>T MANE Select ENSP00000372170.4:n.*61C>T
ENST00000382723.4:c.*61C>T ENSP00000372170.4:n.*61C>T
NM_002448.3:c.*61C>T MANE Select NP_002439.2:n.*61C>T
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