Canonical Allele Identifier: CA1602344955
Gene: MSX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724583C= , CM000667.2:g.174724583C= GRCh38
NC_000005.9:g.174151586C= , CM000667.1:g.174151586C= GRCh37
NC_000005.8:g.174084192C= NCBI36
NG_008124.1:g.5012C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.7:c.-77C= MANE Select ENSP00000239243.5:n.-77C=
ENST00000239243.6:c.-77C= ENSP00000239243.5:n.-77C=
NM_002449.4:c.-77C= NP_002440.2:n.-77C=
NM_001363626.1:c.-77C= NP_001350555.1:n.-77C=
NM_002449.5:c.-77C= MANE Select NP_002440.2:n.-77C=
NM_001363626.2:c.-77C= NP_001350555.1:n.-77C=