Canonical Allele Identifier: CA3711272

Gene: HLA-B

Linked Data

• dbSNP Id: rs748207884
• ExAC: 6:31322936 AACTGCT / A
• gnomAD v2: 6-31322936-AACTGCT-A
• gnomAD v3: 6-31355159-AACTGCT-A
• gnomAD v4: 6-31355159-AACTGCT-A
• MyVariant Identifiers: chr6:g.31322937_31322942del (hg19) ; chr6:g.31355161_31355166del (hg38) ; chr6:g.31355160_31355165del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355161_31355166del , CM000668.2:g.31355161_31355166del	GRCh38
NC_000006.11:g.31322938_31322943del , CM000668.1:g.31322938_31322943del	GRCh37
NC_000006.10:g.31430917_31430922del	NCBI36
NG_023187.1:g.7048_7053del

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3001_3006del
ENST00000481849.6:n.2520_2525del
ENST00000497377.6:n.2427_2432del
ENST00000640094.2:c.895+152_895+157del	ENSP00000491275.2:n.895+152_895+157del
ENST00000696558.1:c.1023_1028del	ENSP00000512716.1:n.1023_1028del
ENST00000696559.1:c.954_959del	ENSP00000512717.1:p.Ala319_Val320del
ENST00000696560.1:c.954_959del	ENSP00000512718.1:p.Ala319_Val320del
ENST00000696561.1:c.954_959del	ENSP00000512719.1:p.Ala319_Val320del
ENST00000696562.1:c.954_959del	ENSP00000512720.1:p.Ala319_Val320del
ENST00000412585.7:c.954_959del MANE Select	ENSP00000399168.2:p.Ala319_Val320del
ENST00000640094.1:c.88+152_88+157del	ENSP00000491275.1:n.88+152_88+157del
ENST00000412585.6:c.954_959del	ENSP00000399168.2:p.Ala319_Val320del
ENST00000463574.1:n.545_550del
NM_005514.6:c.954_959del	NP_005505.2:p.Ala319_Val320del
XM_011514556.1:c.987_992del	XP_011512858.1:p.Ala330_Val331del
XM_011514557.1:c.895+152_895+157del	XP_011512859.1:n.895+152_895+157del
XR_926175.1:n.1393_1398del
NM_005514.7:c.954_959del	NP_005505.2:p.Ala319_Val320del
NM_005514.8:c.954_959del MANE Select	NP_005505.2:p.Ala319_Val320del