Canonical Allele Identifier: CA1602345012
Gene: MSX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724597G= , CM000667.2:g.174724597G= GRCh38
NC_000005.9:g.174151600G= , CM000667.1:g.174151600G= GRCh37
NC_000005.8:g.174084206G= NCBI36
NG_008124.1:g.5026G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.7:c.-63G= MANE Select ENSP00000239243.5:n.-63G=
ENST00000239243.6:c.-63G= ENSP00000239243.5:n.-63G=
NM_002449.4:c.-63G= NP_002440.2:n.-63G=
NM_001363626.1:c.-63G= NP_001350555.1:n.-63G=
NM_002449.5:c.-63G= MANE Select NP_002440.2:n.-63G=
NM_001363626.2:c.-63G= NP_001350555.1:n.-63G=