Canonical Allele Identifier: CA1602344982
Gene: MSX2 HGNC NCBI

Linked Data

dbSNP Id: rs1760729379
gnomAD v4: 5-174724592-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724592A>T , CM000667.2:g.174724592A>T GRCh38
NC_000005.9:g.174151595A>T , CM000667.1:g.174151595A>T GRCh37
NC_000005.8:g.174084201A>T NCBI36
NG_008124.1:g.5021A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.7:c.-68A>T MANE Select ENSP00000239243.5:n.-68A>T
ENST00000239243.6:c.-68A>T ENSP00000239243.5:n.-68A>T
NM_002449.4:c.-68A>T NP_002440.2:n.-68A>T
NM_001363626.1:c.-68A>T NP_001350555.1:n.-68A>T
NM_002449.5:c.-68A>T MANE Select NP_002440.2:n.-68A>T
NM_001363626.2:c.-68A>T NP_001350555.1:n.-68A>T
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