Canonical Allele Identifier: CA2676572722
Gene: MSX2 HGNC NCBI

Linked Data

gnomAD v4: 5-174724645-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724645T>C , CM000667.2:g.174724645T>C GRCh38
NC_000005.9:g.174151648T>C , CM000667.1:g.174151648T>C GRCh37
NC_000005.8:g.174084254T>C NCBI36
NG_008124.1:g.5074T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.7:c.-15T>C MANE Select ENSP00000239243.5:n.-15T>C
ENST00000239243.6:c.-15T>C ENSP00000239243.5:n.-15T>C
ENST00000507785.2:c.-15T>C ENSP00000427425.1:n.-15T>C
NM_002449.4:c.-15T>C NP_002440.2:n.-15T>C
NM_001363626.1:c.-15T>C NP_001350555.1:n.-15T>C
NM_002449.5:c.-15T>C MANE Select NP_002440.2:n.-15T>C
NM_001363626.2:c.-15T>C NP_001350555.1:n.-15T>C
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