Canonical Allele Identifier: CA2677954324

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31354591-GGGGT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354597_31354600del , CM000668.2:g.31354597_31354600del	GRCh38
NC_000006.11:g.31322374_31322377del , CM000668.1:g.31322374_31322377del	GRCh37
NC_000006.10:g.31430353_31430356del	NCBI36
NG_023187.1:g.7618_7621del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3092+38_3092+41del
ENST00000481849.6:n.3052+38_3052+41del
ENST00000497377.6:n.2959+38_2959+41del
ENST00000640094.2:c.928+38_928+41del	ENSP00000491275.2:n.928+38_928+41del
ENST00000696558.1:c.1114+38_1114+41del	ENSP00000512716.1:n.1114+38_1114+41del
ENST00000696559.1:c.1045+38_1045+41del	ENSP00000512717.1:n.1045+38_1045+41del
ENST00000696560.1:c.1045+38_1045+41del	ENSP00000512718.1:n.1045+38_1045+41del
ENST00000696561.1:c.1045+38_1045+41del	ENSP00000512719.1:n.1045+38_1045+41del
ENST00000696562.1:c.1045+38_1045+41del	ENSP00000512720.1:n.1045+38_1045+41del
ENST00000412585.7:c.1045+38_1045+41del MANE Select	ENSP00000399168.2:n.1045+38_1045+41del
ENST00000640094.1:c.121+38_121+41del	ENSP00000491275.1:n.121+38_121+41del
ENST00000412585.6:c.1045+38_1045+41del	ENSP00000399168.2:n.1045+38_1045+41del
ENST00000481849.5:n.212_215del
ENST00000497377.5:n.444+38_444+41del
NM_005514.6:c.1045+38_1045+41del	NP_005505.2:n.1045+38_1045+41del
XM_011514556.1:c.1078+38_1078+41del	XP_011512858.1:n.1078+38_1078+41del
XM_011514557.1:c.928+38_928+41del	XP_011512859.1:n.928+38_928+41del
XR_926175.1:n.1484+38_1484+41del
NM_005514.7:c.1045+38_1045+41del	NP_005505.2:n.1045+38_1045+41del
NM_005514.8:c.1045+38_1045+41del MANE Select	NP_005505.2:n.1045+38_1045+41del