Canonical Allele Identifier: CA2676572657
Gene: MSX2 HGNC NCBI

Linked Data

gnomAD v4: 5-174724584-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724584A>G , CM000667.2:g.174724584A>G GRCh38
NC_000005.9:g.174151587A>G , CM000667.1:g.174151587A>G GRCh37
NC_000005.8:g.174084193A>G NCBI36
NG_008124.1:g.5013A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.7:c.-76A>G MANE Select ENSP00000239243.5:n.-76A>G
ENST00000239243.6:c.-76A>G ENSP00000239243.5:n.-76A>G
NM_002449.4:c.-76A>G NP_002440.2:n.-76A>G
NM_001363626.1:c.-76A>G NP_001350555.1:n.-76A>G
NM_002449.5:c.-76A>G MANE Select NP_002440.2:n.-76A>G
NM_001363626.2:c.-76A>G NP_001350555.1:n.-76A>G
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