Canonical Allele Identifier: CA1602345025
Gene: MSX2 HGNC NCBI

Linked Data

dbSNP Id: rs1760729786
gnomAD v4: 5-174724599-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724599G>A , CM000667.2:g.174724599G>A GRCh38
NC_000005.9:g.174151602G>A , CM000667.1:g.174151602G>A GRCh37
NC_000005.8:g.174084208G>A NCBI36
NG_008124.1:g.5028G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.7:c.-61G>A MANE Select ENSP00000239243.5:n.-61G>A
ENST00000239243.6:c.-61G>A ENSP00000239243.5:n.-61G>A
NM_002449.4:c.-61G>A NP_002440.2:n.-61G>A
NM_001363626.1:c.-61G>A NP_001350555.1:n.-61G>A
NM_002449.5:c.-61G>A MANE Select NP_002440.2:n.-61G>A
NM_001363626.2:c.-61G>A NP_001350555.1:n.-61G>A
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