Canonical Allele Identifier: CA447978200
Gene: MSX2 HGNC NCBI

Linked Data

dbSNP Id: rs1413195221
gnomAD v2: 5-174151689-C-T
gnomAD v4: 5-174724686-C-T
MyVariant Identifiers: chr5:g.174151689C>T (hg19) chr5:g.174724686C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724686C>T , CM000667.2:g.174724686C>T GRCh38
NC_000005.9:g.174151689C>T , CM000667.1:g.174151689C>T GRCh37
NC_000005.8:g.174084295C>T NCBI36
NG_008124.1:g.5115C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.7:c.27C>T MANE Select ENSP00000239243.5:p.Asp9=
ENST00000239243.6:c.27C>T ENSP00000239243.5:p.Asp9=
ENST00000507785.2:c.27C>T ENSP00000427425.1:p.Asp9=
NM_002449.4:c.27C>T NP_002440.2:p.Asp9=
NM_001363626.1:c.27C>T NP_001350555.1:p.Asp9=
NM_002449.5:c.27C>T MANE Select NP_002440.2:p.Asp9=
NM_001363626.2:c.27C>T NP_001350555.1:p.Asp9=
Search 100 bp 5'
Search 100 bp 3'