Canonical Allele Identifier: CA132700874
Gene: MSX2 HGNC NCBI

Linked Data

dbSNP Id: rs924416898
gnomAD v3: 5-174724562-A-G
gnomAD v4: 5-174724562-A-G
MyVariant Identifiers: chr5:g.174151565A>G (hg19) chr5:g.174724562A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724562A>G , CM000667.2:g.174724562A>G GRCh38
NC_000005.9:g.174151565A>G , CM000667.1:g.174151565A>G GRCh37
NC_000005.8:g.174084171A>G NCBI36
NG_008124.1:g.4991A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.6:c.-98A>G ENSP00000239243.5:n.-98A>G
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