Canonical Allele Identifier: CA2677957595

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356686-ACCGGCCTCGCTCTGGTTGTAGTAGCCGCGCAGGTTCCGCAGGCTCTCTCG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356687_31356736del , CM000668.2:g.31356687_31356736del	GRCh38
NC_000006.11:g.31324464_31324513del , CM000668.1:g.31324464_31324513del	GRCh37
NC_000006.10:g.31432443_31432492del	NCBI36
NG_023187.1:g.5477_5526del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1768_1816+1del
ENST00000481849.6:n.1768_1816+1del
ENST00000497377.6:n.1768_1816+1del
ENST00000640094.2:c.295_343+1del
ENST00000696558.1:c.295_343+1del
ENST00000696559.1:c.295_343+1del
ENST00000696560.1:c.295_343+1del
ENST00000696561.1:c.295_343+1del
ENST00000696562.1:c.295_343+1del
ENST00000412585.7:c.295_343+1del
ENST00000412585.6:c.295_343+1del
ENST00000434333.1:c.328_376+1del
ENST00000474381.1:n.170_218+1del
ENST00000498007.1:n.316_365del
ENST00000603274.1:n.41_90del
NM_005514.6:c.295_343+1del
XM_011514556.1:c.328_376+1del
XM_011514557.1:c.295_343+1del
XR_926175.1:n.305_353+1del
NM_005514.7:c.295_343+1del
NM_005514.8:c.295_343+1del