Canonical Allele Identifier: CA1619117006

Gene: HLA-B

Linked Data

• dbSNP Id: rs1554209836
• gnomAD v4: 6-31354440-A-ACCCCCCCCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354443_31354444insCCCCCCCCCC , CM000668.2:g.31354443_31354444insCCCCCCCCCC	GRCh38
NC_000006.11:g.31322220_31322221insCCCCCCCCCC , CM000668.1:g.31322220_31322221insCCCCCCCCCC	GRCh37
NC_000006.10:g.31430199_31430200insCCCCCCCCCC	NCBI36
NG_023187.1:g.7772_7773insGGGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3140+38_3140+39insGGGGGGGGGG
ENST00000481849.6:n.3100+38_3100+39insGGGGGGGGGG
ENST00000497377.6:n.3007+38_3007+39insGGGGGGGGGG
ENST00000696558.1:c.1162+38_1162+39insGGGGGGGGGG	ENSP00000512716.1:n.1162+38_1162+39insGGGGGGGGGG
ENST00000696559.1:c.*4+38_*4+39insGGGGGGGGGG	ENSP00000512717.1:n.*4+38_*4+39insGGGGGGGGGG
ENST00000696560.1:c.*4+38_*4+39insGGGGGGGGGG	ENSP00000512718.1:n.*4+38_*4+39insGGGGGGGGGG
ENST00000696561.1:c.*4+38_*4+39insGGGGGGGGGG	ENSP00000512719.1:n.*4+38_*4+39insGGGGGGGGGG
ENST00000696562.1:c.*4+38_*4+39insGGGGGGGGGG	ENSP00000512720.1:n.*4+38_*4+39insGGGGGGGGGG
ENST00000412585.7:c.*4+38_*4+39insGGGGGGGGGG MANE Select	ENSP00000399168.2:n.*4+38_*4+39insGGGGGGGGGG
ENST00000412585.6:c.*4+38_*4+39insGGGGGGGGGG	ENSP00000399168.2:n.*4+38_*4+39insGGGGGGGGGG
ENST00000481849.5:n.328+38_328+39insGGGGGGGGGG
ENST00000497377.5:n.492+38_492+39insGGGGGGGGGG
NM_005514.6:c.*4+38_*4+39insGGGGGGGGGG	NP_005505.2:n.*4+38_*4+39insGGGGGGGGGG
XM_011514556.1:c.*4+38_*4+39insGGGGGGGGGG	XP_011512858.1:n.*4+38_*4+39insGGGGGGGGGG
XM_011514557.1:c.*4+38_*4+39insGGGGGGGGGG	XP_011512859.1:n.*4+38_*4+39insGGGGGGGGGG
XR_926175.1:n.1532+38_1532+39insGGGGGGGGGG
NM_005514.7:c.*4+38_*4+39insGGGGGGGGGG	NP_005505.2:n.*4+38_*4+39insGGGGGGGGGG
NM_005514.8:c.*4+38_*4+39insGGGGGGGGGG MANE Select	NP_005505.2:n.*4+38_*4+39insGGGGGGGGGG