Canonical Allele Identifier: CA2676572692
Gene: MSX2 HGNC NCBI

Linked Data

gnomAD v4: 5-174724616-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724616G>T , CM000667.2:g.174724616G>T GRCh38
NC_000005.9:g.174151619G>T , CM000667.1:g.174151619G>T GRCh37
NC_000005.8:g.174084225G>T NCBI36
NG_008124.1:g.5045G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.7:c.-44G>T MANE Select ENSP00000239243.5:n.-44G>T
ENST00000239243.6:c.-44G>T ENSP00000239243.5:n.-44G>T
ENST00000507785.2:c.-44G>T ENSP00000427425.1:n.-44G>T
NM_002449.4:c.-44G>T NP_002440.2:n.-44G>T
NM_001363626.1:c.-44G>T NP_001350555.1:n.-44G>T
NM_002449.5:c.-44G>T MANE Select NP_002440.2:n.-44G>T
NM_001363626.2:c.-44G>T NP_001350555.1:n.-44G>T
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