Canonical Allele Identifier: CA1084605789
Gene: MSX2 HGNC NCBI

Linked Data

dbSNP Id: rs1760728331

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724579T>C , CM000667.2:g.174724579T>C GRCh38
NC_000005.9:g.174151582T>C , CM000667.1:g.174151582T>C GRCh37
NC_000005.8:g.174084188T>C NCBI36
NG_008124.1:g.5008T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.6:c.-81T>C ENSP00000239243.5:n.-81T>C
NM_002449.4:c.-81T>C NP_002440.2:n.-81T>C
NM_001363626.1:c.-81T>C NP_001350555.1:n.-81T>C