Canonical Allele Identifier: CA356137417
Gene: MSX1 HGNC NCBI

Linked Data

gnomAD v4: 4-4860125-A-G
MyVariant Identifiers: chr4:g.4861852A>G (hg19) chr4:g.4860125A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4860125A>G , CM000666.2:g.4860125A>G GRCh38
NC_000004.11:g.4861852A>G , CM000666.1:g.4861852A>G GRCh37
NC_000004.10:g.4912753A>G NCBI36
NG_008121.1:g.5461A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000382723.5:c.226A>G MANE Select ENSP00000372170.4:p.Lys76Glu
ENST00000382723.4:c.226A>G ENSP00000372170.4:p.Lys76Glu
NM_002448.3:c.226A>G MANE Select NP_002439.2:p.Lys76Glu
Search 100 bp 5'
Search 100 bp 3'