Canonical Allele Identifier: CA2677953082
Gene: HLA-B HGNC NCBI

Linked Data

gnomAD v4: 6-31354133-GAC-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31354137_31354138del , CM000668.2:g.31354137_31354138del GRCh38
NC_000006.11:g.31321914_31321915del , CM000668.1:g.31321914_31321915del GRCh37
NC_000006.10:g.31429893_31429894del NCBI36
NG_023187.1:g.8078_8079del

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.3302_3303del
ENST00000481849.6:n.3262_3263del
ENST00000497377.6:n.3169_3170del
ENST00000696558.1:c.1324_1325del ENSP00000512716.1:n.1324_1325del
ENST00000696559.1:c.*166_*167del ENSP00000512717.1:n.*166_*167del
ENST00000696560.1:c.*166_*167del ENSP00000512718.1:n.*166_*167del
ENST00000696561.1:c.*166_*167del ENSP00000512719.1:n.*166_*167del
ENST00000696562.1:c.*166_*167del ENSP00000512720.1:n.*166_*167del
ENST00000412585.7:c.*166_*167del MANE Select ENSP00000399168.2:n.*166_*167del
ENST00000412585.6:c.*166_*167del ENSP00000399168.2:n.*166_*167del
ENST00000481849.5:n.490_491del
ENST00000497377.5:n.654_655del
NM_005514.6:c.*166_*167del NP_005505.2:n.*166_*167del
XM_011514556.1:c.*166_*167del XP_011512858.1:n.*166_*167del
XM_011514557.1:c.*166_*167del XP_011512859.1:n.*166_*167del
XR_926175.1:n.1694_1695del
NM_005514.7:c.*166_*167del NP_005505.2:n.*166_*167del
NM_005514.8:c.*166_*167del MANE Select NP_005505.2:n.*166_*167del
Search 100 bp 5'
Search 100 bp 3'