Canonical Allele Identifier: CA2677956842

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356366-G-GTCC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356367_31356368insCCT , CM000668.2:g.31356367_31356368insCCT	GRCh38
NC_000006.11:g.31324144_31324145insCCT , CM000668.1:g.31324144_31324145insCCT	GRCh37
NC_000006.10:g.31432123_31432124insCCT	NCBI36
NG_023187.1:g.5846_5847insGGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1892_1893insGGA
ENST00000481849.6:n.1892_1893insGGA
ENST00000497377.6:n.1892_1893insGGA
ENST00000640094.2:c.419_420insGGA	ENSP00000491275.2:p.Tyr140Ter
ENST00000696558.1:c.419_420insGGA	ENSP00000512716.1:p.Tyr140Ter
ENST00000696559.1:c.419_420insGGA	ENSP00000512717.1:p.Tyr140Ter
ENST00000696560.1:c.419_420insGGA	ENSP00000512718.1:p.Tyr140Ter
ENST00000696561.1:c.419_420insGGA	ENSP00000512719.1:p.Tyr140Ter
ENST00000696562.1:c.419_420insGGA	ENSP00000512720.1:p.Tyr140Ter
ENST00000412585.7:c.419_420insGGA MANE Select	ENSP00000399168.2:p.Tyr140Ter
ENST00000412585.6:c.419_420insGGA	ENSP00000399168.2:p.Tyr140Ter
ENST00000434333.1:c.452_453insGGA	ENSP00000405931.1:p.Tyr151Ter
ENST00000474381.1:n.294_295insGGA
ENST00000498007.1:n.685_686insGGA
NM_005514.6:c.419_420insGGA	NP_005505.2:p.Tyr140Ter
XM_011514556.1:c.452_453insGGA	XP_011512858.1:p.Tyr151Ter
XM_011514557.1:c.419_420insGGA	XP_011512859.1:p.Tyr140Ter
XR_926175.1:n.429_430insGGA
NM_005514.7:c.419_420insGGA	NP_005505.2:p.Tyr140Ter
NM_005514.8:c.419_420insGGA MANE Select	NP_005505.2:p.Tyr140Ter