Canonical Allele Identifier: CA2677954702

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355013-TTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355014_31355015del , CM000668.2:g.31355014_31355015del	GRCh38
NC_000006.11:g.31322791_31322792del , CM000668.1:g.31322791_31322792del	GRCh37
NC_000006.10:g.31430770_31430771del	NCBI36
NG_023187.1:g.7198_7199del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3059+92_3059+93del
ENST00000481849.6:n.2670_2671del
ENST00000497377.6:n.2577_2578del
ENST00000640094.2:c.895+302_895+303del	ENSP00000491275.2:n.895+302_895+303del
ENST00000696558.1:c.1081+92_1081+93del	ENSP00000512716.1:n.1081+92_1081+93del
ENST00000696559.1:c.1012+92_1012+93del	ENSP00000512717.1:n.1012+92_1012+93del
ENST00000696560.1:c.1012+92_1012+93del	ENSP00000512718.1:n.1012+92_1012+93del
ENST00000696561.1:c.1012+92_1012+93del	ENSP00000512719.1:n.1012+92_1012+93del
ENST00000696562.1:c.1012+92_1012+93del	ENSP00000512720.1:n.1012+92_1012+93del
ENST00000412585.7:c.1012+92_1012+93del MANE Select	ENSP00000399168.2:n.1012+92_1012+93del
ENST00000640094.1:c.88+302_88+303del	ENSP00000491275.1:n.88+302_88+303del
ENST00000412585.6:c.1012+92_1012+93del	ENSP00000399168.2:n.1012+92_1012+93del
ENST00000497377.5:n.62_63del
NM_005514.6:c.1012+92_1012+93del	NP_005505.2:n.1012+92_1012+93del
XM_011514556.1:c.1045+92_1045+93del	XP_011512858.1:n.1045+92_1045+93del
XM_011514557.1:c.895+302_895+303del	XP_011512859.1:n.895+302_895+303del
XR_926175.1:n.1451+92_1451+93del
NM_005514.7:c.1012+92_1012+93del	NP_005505.2:n.1012+92_1012+93del
NM_005514.8:c.1012+92_1012+93del MANE Select	NP_005505.2:n.1012+92_1012+93del