Canonical Allele Identifier: CA2677955063

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355162-TGCTAGGACA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355165_31355173del , CM000668.2:g.31355165_31355173del	GRCh38
NC_000006.11:g.31322942_31322950del , CM000668.1:g.31322942_31322950del	GRCh37
NC_000006.10:g.31430921_31430929del	NCBI36
NG_023187.1:g.7042_7050del

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.2995_3003del
ENST00000481849.6:n.2514_2522del
ENST00000497377.6:n.2421_2429del
ENST00000640094.2:c.895+146_895+154del	ENSP00000491275.2:n.895+146_895+154del
ENST00000696558.1:c.1017_1025del	ENSP00000512716.1:n.1017_1025del
ENST00000696559.1:c.948_956del	ENSP00000512717.1:p.Val317_Ala319del
ENST00000696560.1:c.948_956del	ENSP00000512718.1:p.Val317_Ala319del
ENST00000696561.1:c.948_956del	ENSP00000512719.1:p.Val317_Ala319del
ENST00000696562.1:c.948_956del	ENSP00000512720.1:p.Val317_Ala319del
ENST00000412585.7:c.948_956del MANE Select	ENSP00000399168.2:p.Val317_Ala319del
ENST00000640094.1:c.88+146_88+154del	ENSP00000491275.1:n.88+146_88+154del
ENST00000412585.6:c.948_956del	ENSP00000399168.2:p.Val317_Ala319del
ENST00000463574.1:n.539_547del
NM_005514.6:c.948_956del	NP_005505.2:p.Val317_Ala319del
XM_011514556.1:c.981_989del	XP_011512858.1:p.Val328_Ala330del
XM_011514557.1:c.895+146_895+154del	XP_011512859.1:n.895+146_895+154del
XR_926175.1:n.1387_1395del
NM_005514.7:c.948_956del	NP_005505.2:p.Val317_Ala319del
NM_005514.8:c.948_956del MANE Select	NP_005505.2:p.Val317_Ala319del