Canonical Allele Identifier: CA2676572648
Gene: MSX2 HGNC NCBI

Linked Data

gnomAD v4: 5-174724566-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724566C>T , CM000667.2:g.174724566C>T GRCh38
NC_000005.9:g.174151569C>T , CM000667.1:g.174151569C>T GRCh37
NC_000005.8:g.174084175C>T NCBI36
NG_008124.1:g.4995C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.6:c.-94C>T ENSP00000239243.5:n.-94C>T
Search 100 bp 5'
Search 100 bp 3'