Canonical Allele Identifier: CA2677957877

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31357074-A-ACCCCGCACTCACCAGCC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357077_31357078insCGCACTCACCAGCCCCC , CM000668.2:g.31357077_31357078insCGCACTCACCAGCCCCC	GRCh38
NC_000006.11:g.31324854_31324855insCGCACTCACCAGCCCCC , CM000668.1:g.31324854_31324855insCGCACTCACCAGCCCCC	GRCh37
NC_000006.10:g.31432833_31432834insCGCACTCACCAGCCCCC	NCBI36
NG_023187.1:g.5138_5139insGGCTGGTGAGTGCGGGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1546+11_1546+12insGGCTGGTGAGTGCGGGG
ENST00000481849.6:n.1546+11_1546+12insGGCTGGTGAGTGCGGGG
ENST00000497377.6:n.1546+11_1546+12insGGCTGGTGAGTGCGGGG
ENST00000640094.2:c.73+11_73+12insGGCTGGTGAGTGCGGGG	ENSP00000491275.2:n.73+11_73+12insGGCTGGTGAGTGCGGGG
ENST00000696558.1:c.73+11_73+12insGGCTGGTGAGTGCGGGG	ENSP00000512716.1:n.73+11_73+12insGGCTGGTGAGTGCGGGG
ENST00000696559.1:c.73+11_73+12insGGCTGGTGAGTGCGGGG	ENSP00000512717.1:n.73+11_73+12insGGCTGGTGAGTGCGGGG
ENST00000696560.1:c.73+11_73+12insGGCTGGTGAGTGCGGGG	ENSP00000512718.1:n.73+11_73+12insGGCTGGTGAGTGCGGGG
ENST00000696561.1:c.73+11_73+12insGGCTGGTGAGTGCGGGG	ENSP00000512719.1:n.73+11_73+12insGGCTGGTGAGTGCGGGG
ENST00000696562.1:c.73+11_73+12insGGCTGGTGAGTGCGGGG	ENSP00000512720.1:n.73+11_73+12insGGCTGGTGAGTGCGGGG
ENST00000412585.7:c.73+11_73+12insGGCTGGTGAGTGCGGGG MANE Select	ENSP00000399168.2:n.73+11_73+12insGGCTGGTGAGTGCGGGG
ENST00000412585.6:c.73+11_73+12insGGCTGGTGAGTGCGGGG	ENSP00000399168.2:n.73+11_73+12insGGCTGGTGAGTGCGGGG
ENST00000434333.1:c.-12_-11insGGCTGGTGAGTGCGGGG	ENSP00000405931.1:n.-12_-11insGGCTGGTGAGTGCGGGG
ENST00000498007.1:n.94+11_94+12insGGCTGGTGAGTGCGGGG
ENST00000603274.1:n.431_432insCGCACTCACCAGCCCCC
NM_005514.6:c.73+11_73+12insGGCTGGTGAGTGCGGGG	NP_005505.2:n.73+11_73+12insGGCTGGTGAGTGCGGGG
XM_011514556.1:c.-12_-11insGGCTGGTGAGTGCGGGG	XP_011512858.1:n.-12_-11insGGCTGGTGAGTGCGGGG
XM_011514557.1:c.73+11_73+12insGGCTGGTGAGTGCGGGG	XP_011512859.1:n.73+11_73+12insGGCTGGTGAGTGCGGGG
XR_926175.1:n.83+11_83+12insGGCTGGTGAGTGCGGGG
NM_005514.7:c.73+11_73+12insGGCTGGTGAGTGCGGGG	NP_005505.2:n.73+11_73+12insGGCTGGTGAGTGCGGGG
NM_005514.8:c.73+11_73+12insGGCTGGTGAGTGCGGGG MANE Select	NP_005505.2:n.73+11_73+12insGGCTGGTGAGTGCGGGG