Canonical Allele Identifier: CA2833033
Gene: MSX1 HGNC NCBI

Linked Data

dbSNP Id: rs771046674
gnomAD v2: 4-4864369-T-G
gnomAD v4: 4-4862642-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4862642T>G , CM000666.2:g.4862642T>G GRCh38
NC_000004.11:g.4864369T>G , CM000666.1:g.4864369T>G GRCh37
NC_000004.10:g.4915270T>G NCBI36
NG_008121.1:g.7978T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000382723.5:c.470-59T>G MANE Select ENSP00000372170.4:n.470-59T>G
ENST00000382723.4:c.470-59T>G ENSP00000372170.4:n.470-59T>G
ENST00000468421.1:n.181+34T>G
NM_002448.3:c.470-59T>G MANE Select NP_002439.2:n.470-59T>G