Canonical Allele Identifier: CA2403319680
Gene: HMGXB4 HGNC NCBI

Linked Data

dbSNP Id: rs1923334467
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.35267459_35267461del , CM000684.2:g.35267459_35267461del GRCh38
NC_000022.10:g.35663452_35663454del , CM000684.1:g.35663452_35663454del GRCh37
NC_000022.9:g.33993452_33993454del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000216106.6:c.1215+1856_1215+1858del MANE Select ENSP00000216106.5:n.1215+1856_1215+1858de...
ENST00000216106.5:c.1215+1856_1215+1858del ENSP00000216106.5:n.1215+1856_1215+1858de...
ENST00000418170.5:c.*1051+1856_*1051+1858del ENSP00000395532.1:n.*1051+1856_*1051+1858...
NM_001003681.2:c.1215+1856_1215+1858del NP_001003681.1:n.1215+1856_1215+1858del
NR_027780.1:n.1504+1856_1504+1858del
XM_006724100.2:c.1344+1856_1344+1858del XP_006724163.1:n.1344+1856_1344+1858del
XM_006724101.2:c.1344+1856_1344+1858del XP_006724164.1:n.1344+1856_1344+1858del
XM_006724102.1:c.888+1856_888+1858del XP_006724165.1:n.888+1856_888+1858del
XM_011529817.1:c.1215+1856_1215+1858del XP_011528119.1:n.1215+1856_1215+1858del
NM_001362972.1:c.888+1856_888+1858del NP_001349901.1:n.888+1856_888+1858del
XM_006724100.4:c.1344+1856_1344+1858del XP_006724163.1:n.1344+1856_1344+1858del
XM_006724101.4:c.1344+1856_1344+1858del XP_006724164.1:n.1344+1856_1344+1858del
XM_006724102.2:c.888+1856_888+1858del XP_006724165.1:n.888+1856_888+1858del
NM_001003681.3:c.1215+1856_1215+1858del MANE Select NP_001003681.1:n.1215+1856_1215+1858del
NM_001362972.2:c.888+1856_888+1858del NP_001349901.1:n.888+1856_888+1858del
NR_027780.2:n.1463+1856_1463+1858del
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