Canonical Allele Identifier: CA1084605781
Gene: MSX2 HGNC NCBI

Linked Data

dbSNP Id: rs1760727948
gnomAD v4: 5-174724572-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724572T>A , CM000667.2:g.174724572T>A GRCh38
NC_000005.9:g.174151575T>A , CM000667.1:g.174151575T>A GRCh37
NC_000005.8:g.174084181T>A NCBI36
NG_008124.1:g.5001T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.6:c.-88T>A ENSP00000239243.5:n.-88T>A
NM_002449.4:c.-88T>A NP_002440.2:n.-88T>A
NM_001363626.1:c.-88T>A NP_001350555.1:n.-88T>A
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