Canonical Allele Identifier: CA2518027632

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356741-G-GTC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356743_31356744dup , CM000668.2:g.31356743_31356744dup	GRCh38
NC_000006.11:g.31324520_31324521dup , CM000668.1:g.31324520_31324521dup	GRCh37
NC_000006.10:g.31432499_31432500dup	NCBI36
NG_023187.1:g.5470_5471dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1761_1762dup
ENST00000481849.6:n.1761_1762dup
ENST00000497377.6:n.1761_1762dup
ENST00000640094.2:c.288_289dup	ENSP00000491275.2:p.Thr97ArgfsTer?
ENST00000696558.1:c.288_289dup	ENSP00000512716.1:p.Thr97ArgfsTer?
ENST00000696559.1:c.288_289dup	ENSP00000512717.1:p.Thr97ArgfsTer?
ENST00000696560.1:c.288_289dup	ENSP00000512718.1:p.Thr97ArgfsTer?
ENST00000696561.1:c.288_289dup	ENSP00000512719.1:p.Thr97ArgfsTer?
ENST00000696562.1:c.288_289dup	ENSP00000512720.1:p.Thr97ArgfsTer?
ENST00000412585.7:c.288_289dup MANE Select	ENSP00000399168.2:p.Thr97ArgfsTer?
ENST00000412585.6:c.288_289dup	ENSP00000399168.2:p.Thr97ArgfsTer?
ENST00000434333.1:c.321_322dup	ENSP00000405931.1:p.Thr108ArgfsTer?
ENST00000474381.1:n.163_164dup
ENST00000498007.1:n.309_310dup
ENST00000603274.1:n.97_98dup
NM_005514.6:c.288_289dup	NP_005505.2:p.Thr97ArgfsTer?
XM_011514556.1:c.321_322dup	XP_011512858.1:p.Thr108ArgfsTer?
XM_011514557.1:c.288_289dup	XP_011512859.1:p.Thr97ArgfsTer?
XR_926175.1:n.298_299dup
NM_005514.7:c.288_289dup	NP_005505.2:p.Thr97ArgfsTer?
NM_005514.8:c.288_289dup MANE Select	NP_005505.2:p.Thr97ArgfsTer?