Canonical Allele Identifier: CA447978284
Gene: MSX2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.174151731A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724728A>T , CM000667.2:g.174724728A>T GRCh38
NC_000005.9:g.174151731A>T , CM000667.1:g.174151731A>T GRCh37
NC_000005.8:g.174084337A>T NCBI36
NG_008124.1:g.5157A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.7:c.69A>T MANE Select ENSP00000239243.5:p.Gly23=
ENST00000239243.6:c.69A>T ENSP00000239243.5:p.Gly23=
ENST00000507785.2:c.69A>T ENSP00000427425.1:p.Gly23=
NM_002449.4:c.69A>T NP_002440.2:p.Gly23=
NM_001363626.1:c.69A>T NP_001350555.1:p.Gly23=
NM_002449.5:c.69A>T MANE Select NP_002440.2:p.Gly23=
NM_001363626.2:c.69A>T NP_001350555.1:p.Gly23=
Search 100 bp 5'
Search 100 bp 3'