Canonical Allele Identifier: CA1602344891
Gene: MSX2 HGNC NCBI

Linked Data

dbSNP Id: rs1008294376
gnomAD v4: 5-174724569-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724569C>T , CM000667.2:g.174724569C>T GRCh38
NC_000005.9:g.174151572C>T , CM000667.1:g.174151572C>T GRCh37
NC_000005.8:g.174084178C>T NCBI36
NG_008124.1:g.4998C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.6:c.-91C>T ENSP00000239243.5:n.-91C>T
Search 100 bp 5'
Search 100 bp 3'