Canonical Allele Identifier: CA2676572686
Gene: MSX2 HGNC NCBI

Linked Data

gnomAD v4: 5-174724608-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724608G>A , CM000667.2:g.174724608G>A GRCh38
NC_000005.9:g.174151611G>A , CM000667.1:g.174151611G>A GRCh37
NC_000005.8:g.174084217G>A NCBI36
NG_008124.1:g.5037G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.7:c.-52G>A MANE Select ENSP00000239243.5:n.-52G>A
ENST00000239243.6:c.-52G>A ENSP00000239243.5:n.-52G>A
ENST00000507785.2:c.-52G>A ENSP00000427425.1:n.-52G>A
NM_002449.4:c.-52G>A NP_002440.2:n.-52G>A
NM_001363626.1:c.-52G>A NP_001350555.1:n.-52G>A
NM_002449.5:c.-52G>A MANE Select NP_002440.2:n.-52G>A
NM_001363626.2:c.-52G>A NP_001350555.1:n.-52G>A
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