Canonical Allele Identifier: CA2833034
Gene: MSX1 HGNC NCBI

Linked Data

dbSNP Id: rs777060976
gnomAD v2: 4-4864371-A-G
gnomAD v4: 4-4862644-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4862644A>G , CM000666.2:g.4862644A>G GRCh38
NC_000004.11:g.4864371A>G , CM000666.1:g.4864371A>G GRCh37
NC_000004.10:g.4915272A>G NCBI36
NG_008121.1:g.7980A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000382723.5:c.470-57A>G MANE Select ENSP00000372170.4:n.470-57A>G
ENST00000382723.4:c.470-57A>G ENSP00000372170.4:n.470-57A>G
ENST00000468421.1:n.181+36A>G
NM_002448.3:c.470-57A>G MANE Select NP_002439.2:n.470-57A>G