Canonical Allele Identifier: CA1087469628

Gene: HLA-B

Linked Data

• gnomAD v3: 6-31356767-TGTGTTCC-T
• gnomAD v4: 6-31356767-TGTGTTCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356769_31356775del , CM000668.2:g.31356769_31356775del	GRCh38
NC_000006.11:g.31324546_31324552del , CM000668.1:g.31324546_31324552del	GRCh37
NC_000006.10:g.31432525_31432531del	NCBI36
NG_023187.1:g.5439_5445del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1730_1736del
ENST00000481849.6:n.1730_1736del
ENST00000497377.6:n.1730_1736del
ENST00000640094.2:c.257_263del	ENSP00000491275.2:p.Arg86HisfsTer?
ENST00000696558.1:c.257_263del	ENSP00000512716.1:p.Arg86HisfsTer?
ENST00000696559.1:c.257_263del	ENSP00000512717.1:p.Arg86HisfsTer?
ENST00000696560.1:c.257_263del	ENSP00000512718.1:p.Arg86HisfsTer?
ENST00000696561.1:c.257_263del	ENSP00000512719.1:p.Arg86HisfsTer?
ENST00000696562.1:c.257_263del	ENSP00000512720.1:p.Arg86HisfsTer?
ENST00000412585.7:c.257_263del MANE Select	ENSP00000399168.2:p.Arg86HisfsTer?
ENST00000412585.6:c.257_263del	ENSP00000399168.2:p.Arg86HisfsTer?
ENST00000434333.1:c.290_296del	ENSP00000405931.1:p.Arg97HisfsTer?
ENST00000474381.1:n.132_138del
ENST00000498007.1:n.278_284del
ENST00000603274.1:n.123_129del
NM_005514.6:c.257_263del	NP_005505.2:p.Arg86HisfsTer?
XM_011514556.1:c.290_296del	XP_011512858.1:p.Arg97HisfsTer?
XM_011514557.1:c.257_263del	XP_011512859.1:p.Arg86HisfsTer?
XR_926175.1:n.267_273del
NM_005514.7:c.257_263del	NP_005505.2:p.Arg86HisfsTer?
NM_005514.8:c.257_263del MANE Select	NP_005505.2:p.Arg86HisfsTer?