Canonical Allele Identifier: CA2676572647
Gene: MSX2 HGNC NCBI

Linked Data

gnomAD v4: 5-174724565-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724565G>A , CM000667.2:g.174724565G>A GRCh38
NC_000005.9:g.174151568G>A , CM000667.1:g.174151568G>A GRCh37
NC_000005.8:g.174084174G>A NCBI36
NG_008124.1:g.4994G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.6:c.-95G>A ENSP00000239243.5:n.-95G>A
Search 100 bp 5'
Search 100 bp 3'