Canonical Allele Identifier: CA1087469563

Gene: HLA-B

Linked Data

• gnomAD v3: 6-31356759-T-TCCATCCACGGCGCCCGCGGA
• gnomAD v4: 6-31356759-T-TCCATCCACGGCGCCCGCGGA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356759_31356760insCCATCCACGGCGCCCGCGGA , CM000668.2:g.31356759_31356760insCCATCCACGGCGCCCGCGGA	GRCh38
NC_000006.11:g.31324536_31324537insCCATCCACGGCGCCCGCGGA , CM000668.1:g.31324536_31324537insCCATCCACGGCGCCCGCGGA	GRCh37
NC_000006.10:g.31432515_31432516insCCATCCACGGCGCCCGCGGA	NCBI36
NG_023187.1:g.5453_5454insTCCGCGGGCGCCGTGGATGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1744_1745insTCCGCGGGCGCCGTGGATGG
ENST00000481849.6:n.1744_1745insTCCGCGGGCGCCGTGGATGG
ENST00000497377.6:n.1744_1745insTCCGCGGGCGCCGTGGATGG
ENST00000640094.2:c.271_272insTCCGCGGGCGCCGTGGATGG	ENSP00000491275.2:p.Tyr91PhefsTer?
ENST00000696558.1:c.271_272insTCCGCGGGCGCCGTGGATGG	ENSP00000512716.1:p.Tyr91PhefsTer?
ENST00000696559.1:c.271_272insTCCGCGGGCGCCGTGGATGG	ENSP00000512717.1:p.Tyr91PhefsTer?
ENST00000696560.1:c.271_272insTCCGCGGGCGCCGTGGATGG	ENSP00000512718.1:p.Tyr91PhefsTer?
ENST00000696561.1:c.271_272insTCCGCGGGCGCCGTGGATGG	ENSP00000512719.1:p.Tyr91PhefsTer?
ENST00000696562.1:c.271_272insTCCGCGGGCGCCGTGGATGG	ENSP00000512720.1:p.Tyr91PhefsTer?
ENST00000412585.7:c.271_272insTCCGCGGGCGCCGTGGATGG MANE Select	ENSP00000399168.2:p.Tyr91PhefsTer?
ENST00000412585.6:c.271_272insTCCGCGGGCGCCGTGGATGG	ENSP00000399168.2:p.Tyr91PhefsTer?
ENST00000434333.1:c.304_305insTCCGCGGGCGCCGTGGATGG	ENSP00000405931.1:p.Tyr102PhefsTer?
ENST00000474381.1:n.146_147insTCCGCGGGCGCCGTGGATGG
ENST00000498007.1:n.292_293insTCCGCGGGCGCCGTGGATGG
ENST00000603274.1:n.113_114insCCATCCACGGCGCCCGCGGA
NM_005514.6:c.271_272insTCCGCGGGCGCCGTGGATGG	NP_005505.2:p.Tyr91PhefsTer?
XM_011514556.1:c.304_305insTCCGCGGGCGCCGTGGATGG	XP_011512858.1:p.Tyr102PhefsTer?
XM_011514557.1:c.271_272insTCCGCGGGCGCCGTGGATGG	XP_011512859.1:p.Tyr91PhefsTer?
XR_926175.1:n.281_282insTCCGCGGGCGCCGTGGATGG
NM_005514.7:c.271_272insTCCGCGGGCGCCGTGGATGG	NP_005505.2:p.Tyr91PhefsTer?
NM_005514.8:c.271_272insTCCGCGGGCGCCGTGGATGG MANE Select	NP_005505.2:p.Tyr91PhefsTer?