Canonical Allele Identifier: CA356137822
Gene: MSX1 HGNC NCBI

Linked Data

dbSNP Id: rs1737881175
gnomAD v4: 4-4860246-G-T
MyVariant Identifiers: chr4:g.4861973G>T (hg19) chr4:g.4860246G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4860246G>T , CM000666.2:g.4860246G>T GRCh38
NC_000004.11:g.4861973G>T , CM000666.1:g.4861973G>T GRCh37
NC_000004.10:g.4912874G>T NCBI36
NG_008121.1:g.5582G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000382723.5:c.347G>T MANE Select ENSP00000372170.4:p.Gly116Val
ENST00000382723.4:c.347G>T ENSP00000372170.4:p.Gly116Val
NM_002448.3:c.347G>T MANE Select NP_002439.2:p.Gly116Val
Search 100 bp 5'
Search 100 bp 3'