Canonical Allele Identifier: CA823877912

Gene: HLA-B

Linked Data

• dbSNP Id: rs1293509350
• MyVariant Identifiers: chr6:g.31322733_31322734del (hg19) ; chr6:g.31354956_31354957del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354958_31354959del , CM000668.2:g.31354958_31354959del	GRCh38
NC_000006.11:g.31322735_31322736del , CM000668.1:g.31322735_31322736del	GRCh37
NC_000006.10:g.31430714_31430715del	NCBI36
NG_023187.1:g.7256_7257del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3059+150_3059+151del
ENST00000481849.6:n.2728_2729del
ENST00000497377.6:n.2635_2636del
ENST00000640094.2:c.896-292_896-291del	ENSP00000491275.2:n.896-292_896-291del
ENST00000696558.1:c.1081+150_1081+151del	ENSP00000512716.1:n.1081+150_1081+151del
ENST00000696559.1:c.1012+150_1012+151del	ENSP00000512717.1:n.1012+150_1012+151del
ENST00000696560.1:c.1012+150_1012+151del	ENSP00000512718.1:n.1012+150_1012+151del
ENST00000696561.1:c.1012+150_1012+151del	ENSP00000512719.1:n.1012+150_1012+151del
ENST00000696562.1:c.1012+150_1012+151del	ENSP00000512720.1:n.1012+150_1012+151del
ENST00000412585.7:c.1012+150_1012+151del MANE Select	ENSP00000399168.2:n.1012+150_1012+151del
ENST00000640094.1:c.89-292_89-291del	ENSP00000491275.1:n.89-292_89-291del
ENST00000412585.6:c.1012+150_1012+151del	ENSP00000399168.2:n.1012+150_1012+151del
ENST00000497377.5:n.120_121del
NM_005514.6:c.1012+150_1012+151del	NP_005505.2:n.1012+150_1012+151del
XM_011514556.1:c.1045+150_1045+151del	XP_011512858.1:n.1045+150_1045+151del
XM_011514557.1:c.896-292_896-291del	XP_011512859.1:n.896-292_896-291del
XR_926175.1:n.1451+150_1451+151del
NM_005514.7:c.1012+150_1012+151del	NP_005505.2:n.1012+150_1012+151del
NM_005514.8:c.1012+150_1012+151del MANE Select	NP_005505.2:n.1012+150_1012+151del