Canonical Allele Identifier: CA1816330748
Gene: ZHX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.122960853A= , CM000670.2:g.122960853A= GRCh38
NC_000008.10:g.123973093A= , CM000670.1:g.123973093A= GRCh37
NC_000008.9:g.124042274A= NCBI36
NG_046951.1:g.184505A=

Transcript Alleles

HGVS Amino-acid change
ENST00000314393.6:c.*4+6825A= MANE Select ENSP00000314709.4:n.*4+6825A=
ENST00000314393.5:c.*4+6825A= ENSP00000314709.4:n.*4+6825A=
NM_014943.3:c.*4+6825A= NP_055758.1:n.*4+6825A=
XM_005250836.3:c.*4+6825A= XP_005250893.1:n.*4+6825A=
XM_005250837.3:c.*4+6825A= XP_005250894.1:n.*4+6825A=
XM_011516931.1:c.*4+6825A= XP_011515233.1:n.*4+6825A=
XM_011516932.1:c.*4+6825A= XP_011515234.1:n.*4+6825A=
NM_001362797.1:c.*4+6825A= NP_001349726.1:n.*4+6825A=
NM_014943.4:c.*4+6825A= NP_055758.1:n.*4+6825A=
XM_005250836.5:c.*4+6825A= XP_005250893.1:n.*4+6825A=
XM_011516932.3:c.*4+6825A= XP_011515234.1:n.*4+6825A=
NM_014943.5:c.*4+6825A= MANE Select NP_055758.1:n.*4+6825A=
NM_001362797.2:c.*4+6825A= NP_001349726.1:n.*4+6825A=