Canonical Allele Identifier: CA1602344903
Gene: MSX2 HGNC NCBI

Linked Data

dbSNP Id: rs1760728037

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724574C>T , CM000667.2:g.174724574C>T GRCh38
NC_000005.9:g.174151577C>T , CM000667.1:g.174151577C>T GRCh37
NC_000005.8:g.174084183C>T NCBI36
NG_008124.1:g.5003C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.6:c.-86C>T ENSP00000239243.5:n.-86C>T
NM_002449.4:c.-86C>T NP_002440.2:n.-86C>T
NM_001363626.1:c.-86C>T NP_001350555.1:n.-86C>T