Canonical Allele Identifier: CA807837377
Gene: MSX2 HGNC NCBI

Linked Data

dbSNP Id: rs1339392737
MyVariant Identifiers: chr5:g.174151603T>A (hg19) chr5:g.174724600T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724600T>A , CM000667.2:g.174724600T>A GRCh38
NC_000005.9:g.174151603T>A , CM000667.1:g.174151603T>A GRCh37
NC_000005.8:g.174084209T>A NCBI36
NG_008124.1:g.5029T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.7:c.-60T>A MANE Select ENSP00000239243.5:n.-60T>A
ENST00000239243.6:c.-60T>A ENSP00000239243.5:n.-60T>A
NM_002449.4:c.-60T>A NP_002440.2:n.-60T>A
NM_001363626.1:c.-60T>A NP_001350555.1:n.-60T>A
NM_002449.5:c.-60T>A MANE Select NP_002440.2:n.-60T>A
NM_001363626.2:c.-60T>A NP_001350555.1:n.-60T>A
Search 100 bp 5'
Search 100 bp 3'