Canonical Allele Identifier: CA1816330667
Gene: ZHX2 HGNC NCBI

Linked Data

dbSNP Id: rs1230263429

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.122960812G>T , CM000670.2:g.122960812G>T GRCh38
NC_000008.10:g.123973052G>T , CM000670.1:g.123973052G>T GRCh37
NC_000008.9:g.124042233G>T NCBI36
NG_046951.1:g.184464G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000314393.6:c.*4+6784G>T MANE Select ENSP00000314709.4:n.*4+6784G>T
ENST00000314393.5:c.*4+6784G>T ENSP00000314709.4:n.*4+6784G>T
NM_014943.3:c.*4+6784G>T NP_055758.1:n.*4+6784G>T
XM_005250836.3:c.*4+6784G>T XP_005250893.1:n.*4+6784G>T
XM_005250837.3:c.*4+6784G>T XP_005250894.1:n.*4+6784G>T
XM_011516931.1:c.*4+6784G>T XP_011515233.1:n.*4+6784G>T
XM_011516932.1:c.*4+6784G>T XP_011515234.1:n.*4+6784G>T
NM_001362797.1:c.*4+6784G>T NP_001349726.1:n.*4+6784G>T
NM_014943.4:c.*4+6784G>T NP_055758.1:n.*4+6784G>T
XM_005250836.5:c.*4+6784G>T XP_005250893.1:n.*4+6784G>T
XM_011516932.3:c.*4+6784G>T XP_011515234.1:n.*4+6784G>T
NM_014943.5:c.*4+6784G>T MANE Select NP_055758.1:n.*4+6784G>T
NM_001362797.2:c.*4+6784G>T NP_001349726.1:n.*4+6784G>T