Canonical Allele Identifier: CA2677954957

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355128-TCACAGCAGCGAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355135_31355146del , CM000668.2:g.31355135_31355146del	GRCh38
NC_000006.11:g.31322912_31322923del , CM000668.1:g.31322912_31322923del	GRCh37
NC_000006.10:g.31430891_31430902del	NCBI36
NG_023187.1:g.7073_7084del

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3026_3037del
ENST00000481849.6:n.2545_2556del
ENST00000497377.6:n.2452_2463del
ENST00000640094.2:c.895+177_895+188del	ENSP00000491275.2:n.895+177_895+188del
ENST00000696558.1:c.1048_1059del	ENSP00000512716.1:n.1048_1059del
ENST00000696559.1:c.979_990del	ENSP00000512717.1:p.Val327_Val330del
ENST00000696560.1:c.979_990del	ENSP00000512718.1:p.Val327_Val330del
ENST00000696561.1:c.979_990del	ENSP00000512719.1:p.Val327_Val330del
ENST00000696562.1:c.979_990del	ENSP00000512720.1:p.Val327_Val330del
ENST00000412585.7:c.979_990del MANE Select	ENSP00000399168.2:p.Val327_Val330del
ENST00000640094.1:c.88+177_88+188del	ENSP00000491275.1:n.88+177_88+188del
ENST00000412585.6:c.979_990del	ENSP00000399168.2:p.Val327_Val330del
ENST00000463574.1:n.570_581del
NM_005514.6:c.979_990del	NP_005505.2:p.Val327_Val330del
XM_011514556.1:c.1012_1023del	XP_011512858.1:p.Val338_Val341del
XM_011514557.1:c.895+177_895+188del	XP_011512859.1:n.895+177_895+188del
XR_926175.1:n.1418_1429del
NM_005514.7:c.979_990del	NP_005505.2:p.Val327_Val330del
NM_005514.8:c.979_990del MANE Select	NP_005505.2:p.Val327_Val330del