Canonical Allele Identifier: CA136832325

Gene: HLA-B

Linked Data

• dbSNP Id: rs41544518
• gnomAD v2: 6-31322833-AC-A
• gnomAD v4: 6-31355056-AC-A
• MyVariant Identifiers: chr6:g.31322834del (hg19) ; chr6:g.31355057del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355061del , CM000668.2:g.31355061del	GRCh38
NC_000006.11:g.31322838del , CM000668.1:g.31322838del	GRCh37
NC_000006.10:g.31430817del	NCBI36
NG_023187.1:g.7156del

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3059+50del
ENST00000481849.6:n.2628del
ENST00000497377.6:n.2535del
ENST00000640094.2:c.895+260del	ENSP00000491275.2:n.895+260del
ENST00000696558.1:c.1081+50del	ENSP00000512716.1:n.1081+50del
ENST00000696559.1:c.1012+50del	ENSP00000512717.1:n.1012+50del
ENST00000696560.1:c.1012+50del	ENSP00000512718.1:n.1012+50del
ENST00000696561.1:c.1012+50del	ENSP00000512719.1:n.1012+50del
ENST00000696562.1:c.1012+50del	ENSP00000512720.1:n.1012+50del
ENST00000412585.7:c.1012+50del MANE Select	ENSP00000399168.2:n.1012+50del
ENST00000640094.1:c.88+260del	ENSP00000491275.1:n.88+260del
ENST00000412585.6:c.1012+50del	ENSP00000399168.2:n.1012+50del
ENST00000497377.5:n.20del
NM_005514.6:c.1012+50del	NP_005505.2:n.1012+50del
XM_011514556.1:c.1045+50del	XP_011512858.1:n.1045+50del
XM_011514557.1:c.895+260del	XP_011512859.1:n.895+260del
XR_926175.1:n.1451+50del
NM_005514.7:c.1012+50del	NP_005505.2:n.1012+50del
NM_005514.8:c.1012+50del MANE Select	NP_005505.2:n.1012+50del