Canonical Allele Identifier: CA1087464831

Gene: HLA-B

Linked Data

• gnomAD v3: 6-31355219-CGG-C
• gnomAD v4: 6-31355219-CGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355220_31355221del , CM000668.2:g.31355220_31355221del	GRCh38
NC_000006.11:g.31322997_31322998del , CM000668.1:g.31322997_31322998del	GRCh37
NC_000006.10:g.31430976_31430977del	NCBI36
NG_023187.1:g.6992_6993del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2945_2946del
ENST00000481849.6:n.2464_2465del
ENST00000497377.6:n.2371_2372del
ENST00000640094.2:c.895+96_895+97del	ENSP00000491275.2:n.895+96_895+97del
ENST00000696558.1:c.967_968del	ENSP00000512716.1:n.967_968del
ENST00000696559.1:c.898_899del	ENSP00000512717.1:p.Pro300ValfsTer?
ENST00000696560.1:c.898_899del	ENSP00000512718.1:p.Pro300ValfsTer?
ENST00000696561.1:c.898_899del	ENSP00000512719.1:p.Pro300ValfsTer?
ENST00000696562.1:c.898_899del	ENSP00000512720.1:p.Pro300ValfsTer?
ENST00000412585.7:c.898_899del MANE Select	ENSP00000399168.2:p.Pro300ValfsTer?
ENST00000640094.1:c.88+96_88+97del	ENSP00000491275.1:n.88+96_88+97del
ENST00000412585.6:c.898_899del	ENSP00000399168.2:p.Pro300ValfsTer?
ENST00000463574.1:n.489_490del
NM_005514.6:c.898_899del	NP_005505.2:p.Pro300ValfsTer?
XM_011514556.1:c.931_932del	XP_011512858.1:p.Pro311ValfsTer?
XM_011514557.1:c.895+96_895+97del	XP_011512859.1:n.895+96_895+97del
XR_926175.1:n.1337_1338del
NM_005514.7:c.898_899del	NP_005505.2:p.Pro300ValfsTer?
NM_005514.8:c.898_899del MANE Select	NP_005505.2:p.Pro300ValfsTer?