Canonical Allele Identifier: CA136836266

Gene: HLA-B

Linked Data

• dbSNP Id: rs71955092
• gnomAD v2: 6-31324371-GGA-G
• gnomAD v3: 6-31356594-GGA-G
• gnomAD v4: 6-31356594-GGA-G
• COSMIC: COSN1084001
• MyVariant Identifiers: chr6:g.31324372_31324373del (hg19) ; chr6:g.31356595_31356596del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356596_31356597del , CM000668.2:g.31356596_31356597del	GRCh38
NC_000006.11:g.31324373_31324374del , CM000668.1:g.31324373_31324374del	GRCh37
NC_000006.10:g.31432352_31432353del	NCBI36
NG_023187.1:g.5617_5618del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1816+92_1816+93del
ENST00000481849.6:n.1816+92_1816+93del
ENST00000497377.6:n.1816+92_1816+93del
ENST00000640094.2:c.343+92_343+93del	ENSP00000491275.2:n.343+92_343+93del
ENST00000696558.1:c.343+92_343+93del	ENSP00000512716.1:n.343+92_343+93del
ENST00000696559.1:c.343+92_343+93del	ENSP00000512717.1:n.343+92_343+93del
ENST00000696560.1:c.343+92_343+93del	ENSP00000512718.1:n.343+92_343+93del
ENST00000696561.1:c.343+92_343+93del	ENSP00000512719.1:n.343+92_343+93del
ENST00000696562.1:c.343+92_343+93del	ENSP00000512720.1:n.343+92_343+93del
ENST00000412585.7:c.343+92_343+93del MANE Select	ENSP00000399168.2:n.343+92_343+93del
ENST00000412585.6:c.343+92_343+93del	ENSP00000399168.2:n.343+92_343+93del
ENST00000434333.1:c.376+92_376+93del	ENSP00000405931.1:n.376+92_376+93del
ENST00000474381.1:n.218+92_218+93del
ENST00000498007.1:n.456_457del
NM_005514.6:c.343+92_343+93del	NP_005505.2:n.343+92_343+93del
XM_011514556.1:c.376+92_376+93del	XP_011512858.1:n.376+92_376+93del
XM_011514557.1:c.343+92_343+93del	XP_011512859.1:n.343+92_343+93del
XR_926175.1:n.353+92_353+93del
NM_005514.7:c.343+92_343+93del	NP_005505.2:n.343+92_343+93del
NM_005514.8:c.343+92_343+93del MANE Select	NP_005505.2:n.343+92_343+93del