Canonical Allele Identifier: CA136958295
Gene: HCG23 HGNC NCBI
TSBP1-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1057070903
gnomAD v4: 6-32390536-CTT-C
MyVariant Identifiers: chr6:g.32358314_32358315del (hg19) chr6:g.32390537_32390538del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32390539_32390540del , CM000668.2:g.32390539_32390540del GRCh38
NC_000006.11:g.32358316_32358317del , CM000668.1:g.32358316_32358317del GRCh37
NC_000006.10:g.32466294_32466295del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_044996.1:n.30_31del (HCG23)
XM_011515039.1:c.482-14915_482-14914del (TSBP1-AS1) XP_011513341.1:n.482-14915_482-14914del
NR_136245.1:n.303-14915_303-14914del (TSBP1-AS1)
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