Canonical Allele Identifier: CA91668764
Gene: MSX1 HGNC NCBI

Linked Data

dbSNP Id: rs930081770
MyVariant Identifiers: chr4:g.4861976A>T (hg19) chr4:g.4860249A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4860249A>T , CM000666.2:g.4860249A>T GRCh38
NC_000004.11:g.4861976A>T , CM000666.1:g.4861976A>T GRCh37
NC_000004.10:g.4912877A>T NCBI36
NG_008121.1:g.5585A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000382723.5:c.350A>T MANE Select ENSP00000372170.4:p.His117Leu
ENST00000382723.4:c.350A>T ENSP00000372170.4:p.His117Leu
NM_002448.3:c.350A>T MANE Select NP_002439.2:p.His117Leu
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Search 100 bp 3'