Canonical Allele Identifier: CA447978589
Gene: MSX2 HGNC NCBI

Linked Data

dbSNP Id: rs1337378323
gnomAD v2: 5-174151953-G-A
MyVariant Identifiers: chr5:g.174151953G>A (hg19) chr5:g.174724950G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724950G>A , CM000667.2:g.174724950G>A GRCh38
NC_000005.9:g.174151953G>A , CM000667.1:g.174151953G>A GRCh37
NC_000005.8:g.174084559G>A NCBI36
NG_008124.1:g.5379G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.7:c.291G>A MANE Select ENSP00000239243.5:p.Lys97=
ENST00000239243.6:c.291G>A ENSP00000239243.5:p.Lys97=
ENST00000507785.2:c.291G>A ENSP00000427425.1:p.Lys97=
NM_002449.4:c.291G>A NP_002440.2:p.Lys97=
NM_001363626.1:c.291G>A NP_001350555.1:p.Lys97=
NM_002449.5:c.291G>A MANE Select NP_002440.2:p.Lys97=
NM_001363626.2:c.291G>A NP_001350555.1:p.Lys97=
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Search 100 bp 3'