Canonical Allele Identifier: CA2677955523

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355748-CTCCTATTCAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355750_31355759del , CM000668.2:g.31355750_31355759del	GRCh38
NC_000006.11:g.31323527_31323536del , CM000668.1:g.31323527_31323536del	GRCh37
NC_000006.10:g.31431506_31431515del	NCBI36
NG_023187.1:g.6455_6464del

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.2501_2510del
ENST00000481849.6:n.2093-166_2093-157del
ENST00000497377.6:n.2093-166_2093-157del
ENST00000640094.2:c.620-166_620-157del	ENSP00000491275.2:n.620-166_620-157del
ENST00000696558.1:c.668_677del	ENSP00000512716.1:n.[c.668_677del;Asn223A...
ENST00000696559.1:c.620-166_620-157del	ENSP00000512717.1:n.620-166_620-157del
ENST00000696560.1:c.620-166_620-157del	ENSP00000512718.1:n.620-166_620-157del
ENST00000696561.1:c.620-166_620-157del	ENSP00000512719.1:n.620-166_620-157del
ENST00000696562.1:c.620-166_620-157del	ENSP00000512720.1:n.620-166_620-157del
ENST00000412585.7:c.620-166_620-157del MANE Select	ENSP00000399168.2:n.620-166_620-157del
ENST00000412585.6:c.620-166_620-157del	ENSP00000399168.2:n.620-166_620-157del
ENST00000434333.1:c.653-166_653-157del	ENSP00000405931.1:n.653-166_653-157del
ENST00000463574.1:n.45_54del
ENST00000474381.1:n.903_912del
ENST00000498007.1:n.886-166_886-157del
NM_005514.6:c.620-166_620-157del	NP_005505.2:n.620-166_620-157del
XM_011514556.1:c.653-166_653-157del	XP_011512858.1:n.653-166_653-157del
XM_011514557.1:c.620-166_620-157del	XP_011512859.1:n.620-166_620-157del
XR_926175.1:n.1038_1047del
NM_005514.7:c.620-166_620-157del	NP_005505.2:n.620-166_620-157del
NM_005514.8:c.620-166_620-157del MANE Select	NP_005505.2:n.620-166_620-157del