Canonical Allele Identifier: CA2578564582

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356703-TGTA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356708_31356710del , CM000668.2:g.31356708_31356710del	GRCh38
NC_000006.11:g.31324485_31324487del , CM000668.1:g.31324485_31324487del	GRCh37
NC_000006.10:g.31432464_31432466del	NCBI36
NG_023187.1:g.5507_5509del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1798_1800del
ENST00000481849.6:n.1798_1800del
ENST00000497377.6:n.1798_1800del
ENST00000640094.2:c.325_327del	ENSP00000491275.2:p.Tyr109del
ENST00000696558.1:c.325_327del	ENSP00000512716.1:p.Tyr109del
ENST00000696559.1:c.325_327del	ENSP00000512717.1:p.Tyr109del
ENST00000696560.1:c.325_327del	ENSP00000512718.1:p.Tyr109del
ENST00000696561.1:c.325_327del	ENSP00000512719.1:p.Tyr109del
ENST00000696562.1:c.325_327del	ENSP00000512720.1:p.Tyr109del
ENST00000412585.7:c.325_327del MANE Select	ENSP00000399168.2:p.Tyr109del
ENST00000412585.6:c.325_327del	ENSP00000399168.2:p.Tyr109del
ENST00000434333.1:c.358_360del	ENSP00000405931.1:p.Tyr120del
ENST00000474381.1:n.200_202del
ENST00000498007.1:n.346_348del
ENST00000603274.1:n.62_64del
NM_005514.6:c.325_327del	NP_005505.2:p.Tyr109del
XM_011514556.1:c.358_360del	XP_011512858.1:p.Tyr120del
XM_011514557.1:c.325_327del	XP_011512859.1:p.Tyr109del
XR_926175.1:n.335_337del
NM_005514.7:c.325_327del	NP_005505.2:p.Tyr109del
NM_005514.8:c.325_327del MANE Select	NP_005505.2:p.Tyr109del