Canonical Allele Identifier: CA2677957887

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31357082-TCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357084_31357085del , CM000668.2:g.31357084_31357085del	GRCh38
NC_000006.11:g.31324861_31324862del , CM000668.1:g.31324861_31324862del	GRCh37
NC_000006.10:g.31432840_31432841del	NCBI36
NG_023187.1:g.5129_5130del

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1546+2_1546+3del
ENST00000481849.6:n.1546+2_1546+3del
ENST00000497377.6:n.1546+2_1546+3del
ENST00000640094.2:c.73+2_73+3del	ENSP00000491275.2:n.73+2_73+3del
ENST00000696558.1:c.73+2_73+3del	ENSP00000512716.1:n.73+2_73+3del
ENST00000696559.1:c.73+2_73+3del	ENSP00000512717.1:n.73+2_73+3del
ENST00000696560.1:c.73+2_73+3del	ENSP00000512718.1:n.73+2_73+3del
ENST00000696561.1:c.73+2_73+3del	ENSP00000512719.1:n.73+2_73+3del
ENST00000696562.1:c.73+2_73+3del	ENSP00000512720.1:n.73+2_73+3del
ENST00000412585.7:c.73+2_73+3del MANE Select	ENSP00000399168.2:n.73+2_73+3del
ENST00000412585.6:c.73+2_73+3del	ENSP00000399168.2:n.73+2_73+3del
ENST00000434333.1:c.-21_-20del	ENSP00000405931.1:n.-21_-20del
ENST00000498007.1:n.94+2_94+3del
ENST00000603274.1:n.438_439del
NM_005514.6:c.73+2_73+3del	NP_005505.2:n.73+2_73+3del
XM_011514557.1:c.73+2_73+3del	XP_011512859.1:n.73+2_73+3del
XR_926175.1:n.83+2_83+3del
NM_005514.7:c.73+2_73+3del	NP_005505.2:n.73+2_73+3del
NM_005514.8:c.73+2_73+3del MANE Select	NP_005505.2:n.73+2_73+3del