Canonical Allele Identifier: CA1602344970
Gene: MSX2 HGNC NCBI

Linked Data

dbSNP Id: rs1760729160
gnomAD v4: 5-174724586-C-CA
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724592dup , CM000667.2:g.174724592dup GRCh38
NC_000005.9:g.174151595dup , CM000667.1:g.174151595dup GRCh37
NC_000005.8:g.174084201dup NCBI36
NG_008124.1:g.5021dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.7:c.-68dup MANE Select ENSP00000239243.5:n.-68dup
ENST00000239243.6:c.-68dup ENSP00000239243.5:n.-68dup
NM_002449.4:c.-68dup NP_002440.2:n.-68dup
NM_001363626.1:c.-68dup NP_001350555.1:n.-68dup
NM_002449.5:c.-68dup MANE Select NP_002440.2:n.-68dup
NM_001363626.2:c.-68dup NP_001350555.1:n.-68dup
Search 100 bp 5'
Search 100 bp 3'