Canonical Allele Identifier: CA2677957727

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356769-T-TCTGCCG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356769_31356770insCTGCCG , CM000668.2:g.31356769_31356770insCTGCCG	GRCh38
NC_000006.11:g.31324546_31324547insCTGCCG , CM000668.1:g.31324546_31324547insCTGCCG	GRCh37
NC_000006.10:g.31432525_31432526insCTGCCG	NCBI36
NG_023187.1:g.5443_5444insCGGCAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1734_1735insCGGCAG
ENST00000481849.6:n.1734_1735insCGGCAG
ENST00000497377.6:n.1734_1735insCGGCAG
ENST00000640094.2:c.261_262insCGGCAG	ENSP00000491275.2:p.Asn87_Thr88insArgGln
ENST00000696558.1:c.261_262insCGGCAG	ENSP00000512716.1:p.Asn87_Thr88insArgGln
ENST00000696559.1:c.261_262insCGGCAG	ENSP00000512717.1:p.Asn87_Thr88insArgGln
ENST00000696560.1:c.261_262insCGGCAG	ENSP00000512718.1:p.Asn87_Thr88insArgGln
ENST00000696561.1:c.261_262insCGGCAG	ENSP00000512719.1:p.Asn87_Thr88insArgGln
ENST00000696562.1:c.261_262insCGGCAG	ENSP00000512720.1:p.Asn87_Thr88insArgGln
ENST00000412585.7:c.261_262insCGGCAG MANE Select	ENSP00000399168.2:p.Asn87_Thr88insArgGln
ENST00000412585.6:c.261_262insCGGCAG	ENSP00000399168.2:p.Asn87_Thr88insArgGln
ENST00000434333.1:c.294_295insCGGCAG	ENSP00000405931.1:p.Asn98_Thr99insArgGln
ENST00000474381.1:n.136_137insCGGCAG
ENST00000498007.1:n.282_283insCGGCAG
ENST00000603274.1:n.123_124insCTGCCG
NM_005514.6:c.261_262insCGGCAG	NP_005505.2:p.Asn87_Thr88insArgGln
XM_011514556.1:c.294_295insCGGCAG	XP_011512858.1:p.Asn98_Thr99insArgGln
XM_011514557.1:c.261_262insCGGCAG	XP_011512859.1:p.Asn87_Thr88insArgGln
XR_926175.1:n.271_272insCGGCAG
NM_005514.7:c.261_262insCGGCAG	NP_005505.2:p.Asn87_Thr88insArgGln
NM_005514.8:c.261_262insCGGCAG MANE Select	NP_005505.2:p.Asn87_Thr88insArgGln