Canonical Allele Identifier: CA3565150
Gene: MSX2 HGNC NCBI

Linked Data

dbSNP Id: rs756898579
ExAC: 5:174152040 A / G
gnomAD v2: 5-174152040-A-G
gnomAD v4: 5-174725037-A-G
MyVariant Identifiers: chr5:g.174152040A>G (hg19) chr5:g.174725037A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174725037A>G , CM000667.2:g.174725037A>G GRCh38
NC_000005.9:g.174152040A>G , CM000667.1:g.174152040A>G GRCh37
NC_000005.8:g.174084646A>G NCBI36
NG_008124.1:g.5466A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.7:c.378A>G MANE Select ENSP00000239243.5:p.Pro126=
ENST00000239243.6:c.378A>G ENSP00000239243.5:p.Pro126=
ENST00000507785.2:c.378A>G ENSP00000427425.1:p.Pro126=
NM_002449.4:c.378A>G NP_002440.2:p.Pro126=
NM_001363626.1:c.378A>G NP_001350555.1:p.Pro126=
NM_002449.5:c.378A>G MANE Select NP_002440.2:p.Pro126=
NM_001363626.2:c.378A>G NP_001350555.1:p.Pro126=
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