Canonical Allele Identifier: CA3711779

Gene: HLA-B

Linked Data

• dbSNP Id: rs776231854
• ExAC: 6:31324533 TTGTAGA / T
• gnomAD v2: 6-31324533-TTGTAGA-T
• gnomAD v3: 6-31356756-TTGTAGA-T
• gnomAD v4: 6-31356756-TTGTAGA-T
• MyVariant Identifiers: chr6:g.31324534_31324539del (hg19) ; chr6:g.31356757_31356762del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356758_31356763del , CM000668.2:g.31356758_31356763del	GRCh38
NC_000006.11:g.31324535_31324540del , CM000668.1:g.31324535_31324540del	GRCh37
NC_000006.10:g.31432514_31432519del	NCBI36
NG_023187.1:g.5451_5456del

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1742_1747del
ENST00000481849.6:n.1742_1747del
ENST00000497377.6:n.1742_1747del
ENST00000640094.2:c.269_274del	ENSP00000491275.2:p.Ile90_Tyr91del
ENST00000696558.1:c.269_274del	ENSP00000512716.1:p.Ile90_Tyr91del
ENST00000696559.1:c.269_274del	ENSP00000512717.1:p.Ile90_Tyr91del
ENST00000696560.1:c.269_274del	ENSP00000512718.1:p.Ile90_Tyr91del
ENST00000696561.1:c.269_274del	ENSP00000512719.1:p.Ile90_Tyr91del
ENST00000696562.1:c.269_274del	ENSP00000512720.1:p.Ile90_Tyr91del
ENST00000412585.7:c.269_274del MANE Select	ENSP00000399168.2:p.Ile90_Tyr91del
ENST00000412585.6:c.269_274del	ENSP00000399168.2:p.Ile90_Tyr91del
ENST00000434333.1:c.302_307del	ENSP00000405931.1:p.Ile101_Tyr102del
ENST00000474381.1:n.144_149del
ENST00000498007.1:n.290_295del
ENST00000603274.1:n.112_117del
NM_005514.6:c.269_274del	NP_005505.2:p.Ile90_Tyr91del
XM_011514556.1:c.302_307del	XP_011512858.1:p.Ile101_Tyr102del
XM_011514557.1:c.269_274del	XP_011512859.1:p.Ile90_Tyr91del
XR_926175.1:n.279_284del
NM_005514.7:c.269_274del	NP_005505.2:p.Ile90_Tyr91del
NM_005514.8:c.269_274del MANE Select	NP_005505.2:p.Ile90_Tyr91del