Canonical Allele Identifier: CA1087467319

Gene: HLA-B

Linked Data

• gnomAD v3: 6-31356165-ACCAGCGCGCTCCAGCTTGTCCTTCCCGTTCTCCAGGTATCTGCGGAGCCACTCCACGCACTCGCCCTCCAGGTAGGCTCTCCGCTGCTCCGCCTCACGGGCCGCCTCCCACTTGCGCTGGGTGATCTGAGCCGCCGTGTCCGCGGCGGTCCAGGAGCGCAGGTCCTCGTTCAGGGCGATGTAATCCTTGCCGTCGTAGGCGTACTGGTCATG-A
• gnomAD v4: 6-31356165-ACCAGCGCGCTCCAGCTTGTCCTTCCCGTTCTCCAGGTATCTGCGGAGCCACTCCACGCACTCGCCCTCCAGGTAGGCTCTCCGCTGCTCCGCCTCACGGGCCGCCTCCCACTTGCGCTGGGTGATCTGAGCCGCCGTGTCCGCGGCGGTCCAGGAGCGCAGGTCCTCGTTCAGGGCGATGTAATCCTTGCCGTCGTAGGCGTACTGGTCATG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356168_31356379del , CM000668.2:g.31356168_31356379del	GRCh38
NC_000006.11:g.31323945_31324156del , CM000668.1:g.31323945_31324156del	GRCh37
NC_000006.10:g.31431924_31432135del	NCBI36
NG_023187.1:g.5836_6047del

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1882_2093del
ENST00000481849.6:n.1882_2092+1del
ENST00000497377.6:n.1882_2092+1del
ENST00000640094.2:c.409_619+1del
ENST00000696558.1:c.409_619+1del
ENST00000696559.1:c.409_619+1del
ENST00000696560.1:c.409_619+1del
ENST00000696561.1:c.409_619+1del
ENST00000696562.1:c.409_619+1del
ENST00000412585.7:c.409_619+1del
ENST00000412585.6:c.409_619+1del
ENST00000434333.1:c.442_652+1del
ENST00000474381.1:n.284_495del
ENST00000498007.1:n.675_885+1del
NM_005514.6:c.409_619+1del
XM_011514556.1:c.442_652+1del
XM_011514557.1:c.409_619+1del
XR_926175.1:n.419_630del
NM_005514.7:c.409_619+1del
NM_005514.8:c.409_619+1del