Canonical Allele Identifier: CA2677953863

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31354431-C-CCCCCCCCA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354431_31354432insCCCCCCCA , CM000668.2:g.31354431_31354432insCCCCCCCA	GRCh38
NC_000006.11:g.31322208_31322209insCCCCCCCA , CM000668.1:g.31322208_31322209insCCCCCCCA	GRCh37
NC_000006.10:g.31430187_31430188insCCCCCCCA	NCBI36
NG_023187.1:g.7781_7782insTGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3140+47_3140+48insTGGGGGGG
ENST00000481849.6:n.3100+47_3100+48insTGGGGGGG
ENST00000497377.6:n.3007+47_3007+48insTGGGGGGG
ENST00000696558.1:c.1162+47_1162+48insTGGGGGGG	ENSP00000512716.1:n.1162+47_1162+48insTGGGGGGG
ENST00000696559.1:c.*4+47_*4+48insTGGGGGGG	ENSP00000512717.1:n.*4+47_*4+48insTGGGGGGG
ENST00000696560.1:c.*4+47_*4+48insTGGGGGGG	ENSP00000512718.1:n.*4+47_*4+48insTGGGGGGG
ENST00000696561.1:c.*4+47_*4+48insTGGGGGGG	ENSP00000512719.1:n.*4+47_*4+48insTGGGGGGG
ENST00000696562.1:c.*4+47_*4+48insTGGGGGGG	ENSP00000512720.1:n.*4+47_*4+48insTGGGGGGG
ENST00000412585.7:c.*4+47_*4+48insTGGGGGGG MANE Select	ENSP00000399168.2:n.*4+47_*4+48insTGGGGGGG
ENST00000412585.6:c.*4+47_*4+48insTGGGGGGG	ENSP00000399168.2:n.*4+47_*4+48insTGGGGGGG
ENST00000481849.5:n.328+47_328+48insTGGGGGGG
ENST00000497377.5:n.492+47_492+48insTGGGGGGG
NM_005514.6:c.*4+47_*4+48insTGGGGGGG	NP_005505.2:n.*4+47_*4+48insTGGGGGGG
XM_011514556.1:c.*4+47_*4+48insTGGGGGGG	XP_011512858.1:n.*4+47_*4+48insTGGGGGGG
XM_011514557.1:c.*4+47_*4+48insTGGGGGGG	XP_011512859.1:n.*4+47_*4+48insTGGGGGGG
XR_926175.1:n.1532+47_1532+48insTGGGGGGG
NM_005514.7:c.*4+47_*4+48insTGGGGGGG	NP_005505.2:n.*4+47_*4+48insTGGGGGGG
NM_005514.8:c.*4+47_*4+48insTGGGGGGG MANE Select	NP_005505.2:n.*4+47_*4+48insTGGGGGGG