Canonical Allele Identifier: CA566689269

Gene: HLA-B

Linked Data

• gnomAD v2: 6-31324062-GGTGAT-G
• gnomAD v4: 6-31356285-GGTGAT-G
• MyVariant Identifiers: chr6:g.31324063_31324067del (hg19) ; chr6:g.31356286_31356290del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356286_31356290del , CM000668.2:g.31356286_31356290del	GRCh38
NC_000006.11:g.31324063_31324067del , CM000668.1:g.31324063_31324067del	GRCh37
NC_000006.10:g.31432042_31432046del	NCBI36
NG_023187.1:g.5923_5927del

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1969_1973del
ENST00000481849.6:n.1969_1973del
ENST00000497377.6:n.1969_1973del
ENST00000640094.2:c.496_500del	ENSP00000491275.2:p.Ile166ProfsTer9
ENST00000696558.1:c.496_500del	ENSP00000512716.1:p.Ile166ProfsTer9
ENST00000696559.1:c.496_500del	ENSP00000512717.1:p.Ile166ProfsTer9
ENST00000696560.1:c.496_500del	ENSP00000512718.1:p.Ile166ProfsTer9
ENST00000696561.1:c.496_500del	ENSP00000512719.1:p.Ile166ProfsTer9
ENST00000696562.1:c.496_500del	ENSP00000512720.1:p.Ile166ProfsTer9
ENST00000412585.7:c.496_500del MANE Select	ENSP00000399168.2:p.Ile166ProfsTer9
ENST00000412585.6:c.496_500del	ENSP00000399168.2:p.Ile166ProfsTer9
ENST00000434333.1:c.529_533del	ENSP00000405931.1:p.Ile177ProfsTer9
ENST00000474381.1:n.371_375del
ENST00000498007.1:n.762_766del
NM_005514.6:c.496_500del	NP_005505.2:p.Ile166ProfsTer9
XM_011514556.1:c.529_533del	XP_011512858.1:p.Ile177ProfsTer9
XM_011514557.1:c.496_500del	XP_011512859.1:p.Ile166ProfsTer9
XR_926175.1:n.506_510del
NM_005514.7:c.496_500del	NP_005505.2:p.Ile166ProfsTer9
NM_005514.8:c.496_500del MANE Select	NP_005505.2:p.Ile166ProfsTer9