Canonical Allele Identifier: CA2677954340

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31354622-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354622_31354623insT , CM000668.2:g.31354622_31354623insT	GRCh38
NC_000006.11:g.31322399_31322400insT , CM000668.1:g.31322399_31322400insT	GRCh37
NC_000006.10:g.31430378_31430379insT	NCBI36
NG_023187.1:g.7590_7591insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3092+10_3092+11insA
ENST00000481849.6:n.3052+10_3052+11insA
ENST00000497377.6:n.2959+10_2959+11insA
ENST00000640094.2:c.928+10_928+11insA	ENSP00000491275.2:n.928+10_928+11insA
ENST00000696558.1:c.1114+10_1114+11insA	ENSP00000512716.1:n.1114+10_1114+11insA
ENST00000696559.1:c.1045+10_1045+11insA	ENSP00000512717.1:n.1045+10_1045+11insA
ENST00000696560.1:c.1045+10_1045+11insA	ENSP00000512718.1:n.1045+10_1045+11insA
ENST00000696561.1:c.1045+10_1045+11insA	ENSP00000512719.1:n.1045+10_1045+11insA
ENST00000696562.1:c.1045+10_1045+11insA	ENSP00000512720.1:n.1045+10_1045+11insA
ENST00000412585.7:c.1045+10_1045+11insA MANE Select	ENSP00000399168.2:n.1045+10_1045+11insA
ENST00000640094.1:c.121+10_121+11insA	ENSP00000491275.1:n.121+10_121+11insA
ENST00000412585.6:c.1045+10_1045+11insA	ENSP00000399168.2:n.1045+10_1045+11insA
ENST00000481849.5:n.184_185insA
ENST00000497377.5:n.444+10_444+11insA
NM_005514.6:c.1045+10_1045+11insA	NP_005505.2:n.1045+10_1045+11insA
XM_011514556.1:c.1078+10_1078+11insA	XP_011512858.1:n.1078+10_1078+11insA
XM_011514557.1:c.928+10_928+11insA	XP_011512859.1:n.928+10_928+11insA
XR_926175.1:n.1484+10_1484+11insA
NM_005514.7:c.1045+10_1045+11insA	NP_005505.2:n.1045+10_1045+11insA
NM_005514.8:c.1045+10_1045+11insA MANE Select	NP_005505.2:n.1045+10_1045+11insA