Canonical Allele Identifier: CA823878086

Gene: HLA-B

Linked Data

• dbSNP Id: rs1438019665
• gnomAD v3: 6-31355146-CTCCGAT-C
• gnomAD v4: 6-31355146-CTCCGAT-C
• MyVariant Identifiers: chr6:g.31322924_31322929del (hg19) ; chr6:g.31355147_31355152del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355147_31355152del , CM000668.2:g.31355147_31355152del	GRCh38
NC_000006.11:g.31322924_31322929del , CM000668.1:g.31322924_31322929del	GRCh37
NC_000006.10:g.31430903_31430908del	NCBI36
NG_023187.1:g.7061_7066del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3014_3019del
ENST00000481849.6:n.2533_2538del
ENST00000497377.6:n.2440_2445del
ENST00000640094.2:c.895+165_895+170del	ENSP00000491275.2:n.895+165_895+170del
ENST00000696558.1:c.1036_1041del	ENSP00000512716.1:n.1036_1041del
ENST00000696559.1:c.967_972del	ENSP00000512717.1:p.Ile323_Gly324del
ENST00000696560.1:c.967_972del	ENSP00000512718.1:p.Ile323_Gly324del
ENST00000696561.1:c.967_972del	ENSP00000512719.1:p.Ile323_Gly324del
ENST00000696562.1:c.967_972del	ENSP00000512720.1:p.Ile323_Gly324del
ENST00000412585.7:c.967_972del MANE Select	ENSP00000399168.2:p.Ile323_Gly324del
ENST00000640094.1:c.88+165_88+170del	ENSP00000491275.1:n.88+165_88+170del
ENST00000412585.6:c.967_972del	ENSP00000399168.2:p.Ile323_Gly324del
ENST00000463574.1:n.558_563del
NM_005514.6:c.967_972del	NP_005505.2:p.Ile323_Gly324del
XM_011514556.1:c.1000_1005del	XP_011512858.1:p.Ile334_Gly335del
XM_011514557.1:c.895+165_895+170del	XP_011512859.1:n.895+165_895+170del
XR_926175.1:n.1406_1411del
NM_005514.7:c.967_972del	NP_005505.2:p.Ile323_Gly324del
NM_005514.8:c.967_972del MANE Select	NP_005505.2:p.Ile323_Gly324del