Canonical Allele Identifier: CA566340055

Gene: HLA-B

Linked Data

• dbSNP Id: rs1766649699
• gnomAD v2: 6-31321807-GTA-G
• gnomAD v3: 6-31354030-GTA-G
• gnomAD v4: 6-31354030-GTA-G
• MyVariant Identifiers: chr6:g.31321808_31321809del (hg19) ; chr6:g.31354031_31354032del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354031_31354032del , CM000668.2:g.31354031_31354032del	GRCh38
NC_000006.11:g.31321808_31321809del , CM000668.1:g.31321808_31321809del	GRCh37
NC_000006.10:g.31429787_31429788del	NCBI36
NG_023187.1:g.8181_8182del

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3405_3406del
ENST00000481849.6:n.3365_3366del
ENST00000497377.6:n.3272_3273del
ENST00000696558.1:c.1427_1428del	ENSP00000512716.1:n.1427_1428del
ENST00000696559.1:c.*269_*270del	ENSP00000512717.1:n.*269_*270del
ENST00000696560.1:c.*269_*270del	ENSP00000512718.1:n.*269_*270del
ENST00000696561.1:c.*269_*270del	ENSP00000512719.1:n.*269_*270del
ENST00000696562.1:c.*269_*270del	ENSP00000512720.1:n.*269_*270del
ENST00000412585.7:c.*269_*270del MANE Select	ENSP00000399168.2:n.*269_*270del
ENST00000412585.6:c.*269_*270del	ENSP00000399168.2:n.*269_*270del
ENST00000481849.5:n.593_594del
ENST00000497377.5:n.757_758del
NM_005514.6:c.*269_*270del	NP_005505.2:n.*269_*270del
XM_011514556.1:c.*269_*270del	XP_011512858.1:n.*269_*270del
XM_011514557.1:c.*269_*270del	XP_011512859.1:n.*269_*270del
XR_926175.1:n.1797_1798del
NM_005514.7:c.*269_*270del	NP_005505.2:n.*269_*270del
NM_005514.8:c.*269_*270del MANE Select	NP_005505.2:n.*269_*270del