Canonical Allele Identifier: CA2677957839

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356986-CCG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356987_31356988del , CM000668.2:g.31356987_31356988del	GRCh38
NC_000006.11:g.31324764_31324765del , CM000668.1:g.31324764_31324765del	GRCh37
NC_000006.10:g.31432743_31432744del	NCBI36
NG_023187.1:g.5225_5226del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1547-31_1547-30del
ENST00000481849.6:n.1547-31_1547-30del
ENST00000497377.6:n.1547-31_1547-30del
ENST00000640094.2:c.74-31_74-30del	ENSP00000491275.2:n.74-31_74-30del
ENST00000696558.1:c.74-31_74-30del	ENSP00000512716.1:n.74-31_74-30del
ENST00000696559.1:c.74-31_74-30del	ENSP00000512717.1:n.74-31_74-30del
ENST00000696560.1:c.74-31_74-30del	ENSP00000512718.1:n.74-31_74-30del
ENST00000696561.1:c.74-31_74-30del	ENSP00000512719.1:n.74-31_74-30del
ENST00000696562.1:c.74-31_74-30del	ENSP00000512720.1:n.74-31_74-30del
ENST00000412585.7:c.74-31_74-30del MANE Select	ENSP00000399168.2:n.74-31_74-30del
ENST00000412585.6:c.74-31_74-30del	ENSP00000399168.2:n.74-31_74-30del
ENST00000434333.1:c.76_77del	ENSP00000405931.1:p.Arg26GlyfsTer?
ENST00000498007.1:n.95-31_95-30del
ENST00000603274.1:n.341_342del
NM_005514.6:c.74-31_74-30del	NP_005505.2:n.74-31_74-30del
XM_011514556.1:c.76_77del	XP_011512858.1:p.Arg26GlyfsTer?
XM_011514557.1:c.74-31_74-30del	XP_011512859.1:n.74-31_74-30del
XR_926175.1:n.84-31_84-30del
NM_005514.7:c.74-31_74-30del	NP_005505.2:n.74-31_74-30del
NM_005514.8:c.74-31_74-30del MANE Select	NP_005505.2:n.74-31_74-30del