Canonical Allele Identifier: CA2676572645
Gene: MSX2 HGNC NCBI

Linked Data

gnomAD v4: 5-174724564-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724564C>A , CM000667.2:g.174724564C>A GRCh38
NC_000005.9:g.174151567C>A , CM000667.1:g.174151567C>A GRCh37
NC_000005.8:g.174084173C>A NCBI36
NG_008124.1:g.4993C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.6:c.-96C>A ENSP00000239243.5:n.-96C>A
Search 100 bp 5'
Search 100 bp 3'