Canonical Allele Identifier: CA1058779102
Gene: MSX1 HGNC NCBI

Linked Data

dbSNP Id: rs1737943176
gnomAD v3: 4-4862641-C-G
gnomAD v4: 4-4862641-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4862641C>G , CM000666.2:g.4862641C>G GRCh38
NC_000004.11:g.4864368C>G , CM000666.1:g.4864368C>G GRCh37
NC_000004.10:g.4915269C>G NCBI36
NG_008121.1:g.7977C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000382723.5:c.470-60C>G MANE Select ENSP00000372170.4:n.470-60C>G
ENST00000382723.4:c.470-60C>G ENSP00000372170.4:n.470-60C>G
ENST00000468421.1:n.181+33C>G
NM_002448.3:c.470-60C>G MANE Select NP_002439.2:n.470-60C>G