Canonical Allele Identifier: CA1816330658
Gene: ZHX2 HGNC NCBI

Linked Data

dbSNP Id: rs1813422751

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.122960809C>A , CM000670.2:g.122960809C>A GRCh38
NC_000008.10:g.123973049C>A , CM000670.1:g.123973049C>A GRCh37
NC_000008.9:g.124042230C>A NCBI36
NG_046951.1:g.184461C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000314393.6:c.*4+6781C>A MANE Select ENSP00000314709.4:n.*4+6781C>A
ENST00000314393.5:c.*4+6781C>A ENSP00000314709.4:n.*4+6781C>A
NM_014943.3:c.*4+6781C>A NP_055758.1:n.*4+6781C>A
XM_005250836.3:c.*4+6781C>A XP_005250893.1:n.*4+6781C>A
XM_005250837.3:c.*4+6781C>A XP_005250894.1:n.*4+6781C>A
XM_011516931.1:c.*4+6781C>A XP_011515233.1:n.*4+6781C>A
XM_011516932.1:c.*4+6781C>A XP_011515234.1:n.*4+6781C>A
NM_001362797.1:c.*4+6781C>A NP_001349726.1:n.*4+6781C>A
NM_014943.4:c.*4+6781C>A NP_055758.1:n.*4+6781C>A
XM_005250836.5:c.*4+6781C>A XP_005250893.1:n.*4+6781C>A
XM_011516932.3:c.*4+6781C>A XP_011515234.1:n.*4+6781C>A
NM_014943.5:c.*4+6781C>A MANE Select NP_055758.1:n.*4+6781C>A
NM_001362797.2:c.*4+6781C>A NP_001349726.1:n.*4+6781C>A