Canonical Allele Identifier: CA1087459692

Gene: HLA-B

Linked Data

• dbSNP Id: rs1766656706
• gnomAD v3: 6-31354088-A-AT
• gnomAD v4: 6-31354088-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354088_31354089insT , CM000668.2:g.31354088_31354089insT	GRCh38
NC_000006.11:g.31321865_31321866insT , CM000668.1:g.31321865_31321866insT	GRCh37
NC_000006.10:g.31429844_31429845insT	NCBI36
NG_023187.1:g.8124_8125insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3348_3349insA
ENST00000481849.6:n.3308_3309insA
ENST00000497377.6:n.3215_3216insA
ENST00000696558.1:c.1370_1371insA	ENSP00000512716.1:n.1370_1371insA
ENST00000696559.1:c.*212_*213insA	ENSP00000512717.1:n.*212_*213insA
ENST00000696560.1:c.*212_*213insA	ENSP00000512718.1:n.*212_*213insA
ENST00000696561.1:c.*212_*213insA	ENSP00000512719.1:n.*212_*213insA
ENST00000696562.1:c.*212_*213insA	ENSP00000512720.1:n.*212_*213insA
ENST00000412585.7:c.*212_*213insA MANE Select	ENSP00000399168.2:n.*212_*213insA
ENST00000412585.6:c.*212_*213insA	ENSP00000399168.2:n.*212_*213insA
ENST00000481849.5:n.536_537insA
ENST00000497377.5:n.700_701insA
NM_005514.6:c.*212_*213insA	NP_005505.2:n.*212_*213insA
XM_011514556.1:c.*212_*213insA	XP_011512858.1:n.*212_*213insA
XM_011514557.1:c.*212_*213insA	XP_011512859.1:n.*212_*213insA
XR_926175.1:n.1740_1741insA
NM_005514.7:c.*212_*213insA	NP_005505.2:n.*212_*213insA
NM_005514.8:c.*212_*213insA MANE Select	NP_005505.2:n.*212_*213insA