Canonical Allele Identifier: CA132700885
Gene: MSX2 HGNC NCBI

Linked Data

dbSNP Id: rs982499616
MyVariant Identifiers: chr5:g.174151593A>G (hg19) chr5:g.174724590A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724590A>G , CM000667.2:g.174724590A>G GRCh38
NC_000005.9:g.174151593A>G , CM000667.1:g.174151593A>G GRCh37
NC_000005.8:g.174084199A>G NCBI36
NG_008124.1:g.5019A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.7:c.-70A>G MANE Select ENSP00000239243.5:n.-70A>G
ENST00000239243.6:c.-70A>G ENSP00000239243.5:n.-70A>G
NM_002449.4:c.-70A>G NP_002440.2:n.-70A>G
NM_001363626.1:c.-70A>G NP_001350555.1:n.-70A>G
NM_002449.5:c.-70A>G MANE Select NP_002440.2:n.-70A>G
NM_001363626.2:c.-70A>G NP_001350555.1:n.-70A>G
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