Canonical Allele Identifier: CA91671076
Gene: MSX1 HGNC NCBI

Linked Data

dbSNP Id: rs921038979
MyVariant Identifiers: chr4:g.4863997C>T (hg19) chr4:g.4862270C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4862270C>T , CM000666.2:g.4862270C>T GRCh38
NC_000004.11:g.4863997C>T , CM000666.1:g.4863997C>T GRCh37
NC_000004.10:g.4914898C>T NCBI36
NG_008121.1:g.7606C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.470-431C>T MANE Select ENSP00000372170.4:n.470-431C>T
ENST00000382723.4:c.470-431C>T ENSP00000372170.4:n.470-431C>T
NM_002448.3:c.470-431C>T MANE Select NP_002439.2:n.470-431C>T
Search 100 bp 5'
Search 100 bp 3'