Canonical Allele Identifier: CA2578488455
Gene: MSX2 HGNC NCBI

Linked Data

gnomAD v4: 5-174724568-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724568C>T , CM000667.2:g.174724568C>T GRCh38
NC_000005.9:g.174151571C>T , CM000667.1:g.174151571C>T GRCh37
NC_000005.8:g.174084177C>T NCBI36
NG_008124.1:g.4997C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.6:c.-92C>T ENSP00000239243.5:n.-92C>T
Search 100 bp 5'
Search 100 bp 3'