Canonical Allele Identifier: CA1619112991

Gene: HLA-B

Linked Data

• dbSNP Id: rs1767082278
• gnomAD v4: 6-31356747-GCCTGGGCCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356748_31356756del , CM000668.2:g.31356748_31356756del	GRCh38
NC_000006.11:g.31324525_31324533del , CM000668.1:g.31324525_31324533del	GRCh37
NC_000006.10:g.31432504_31432512del	NCBI36
NG_023187.1:g.5457_5465del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1748_1756del
ENST00000481849.6:n.1748_1756del
ENST00000497377.6:n.1748_1756del
ENST00000640094.2:c.275_283del	ENSP00000491275.2:p.Lys92_Ala95delinsThr
ENST00000696558.1:c.275_283del	ENSP00000512716.1:p.Lys92_Ala95delinsThr
ENST00000696559.1:c.275_283del	ENSP00000512717.1:p.Lys92_Ala95delinsThr
ENST00000696560.1:c.275_283del	ENSP00000512718.1:p.Lys92_Ala95delinsThr
ENST00000696561.1:c.275_283del	ENSP00000512719.1:p.Lys92_Ala95delinsThr
ENST00000696562.1:c.275_283del	ENSP00000512720.1:p.Lys92_Ala95delinsThr
ENST00000412585.7:c.275_283del MANE Select	ENSP00000399168.2:p.Lys92_Ala95delinsThr
ENST00000412585.6:c.275_283del	ENSP00000399168.2:p.Lys92_Ala95delinsThr
ENST00000434333.1:c.308_316del	ENSP00000405931.1:p.Lys103_Ala106delinsThr
ENST00000474381.1:n.150_158del
ENST00000498007.1:n.296_304del
ENST00000603274.1:n.102_110del
NM_005514.6:c.275_283del	NP_005505.2:p.Lys92_Ala95delinsThr
XM_011514556.1:c.308_316del	XP_011512858.1:p.Lys103_Ala106delinsThr
XM_011514557.1:c.275_283del	XP_011512859.1:p.Lys92_Ala95delinsThr
XR_926175.1:n.285_293del
NM_005514.7:c.275_283del	NP_005505.2:p.Lys92_Ala95delinsThr
NM_005514.8:c.275_283del MANE Select	NP_005505.2:p.Lys92_Ala95delinsThr