Canonical Allele Identifier: CA823877920

Gene: HLA-B

Linked Data

• dbSNP Id: rs1446955505
• gnomAD v4: 6-31354973-ACAGGGTCC-A
• MyVariant Identifiers: chr6:g.31322751_31322758del (hg19) ; chr6:g.31354974_31354981del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354978_31354985del , CM000668.2:g.31354978_31354985del	GRCh38
NC_000006.11:g.31322755_31322762del , CM000668.1:g.31322755_31322762del	GRCh37
NC_000006.10:g.31430734_31430741del	NCBI36
NG_023187.1:g.7232_7239del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3059+126_3059+133del
ENST00000481849.6:n.2704_2711del
ENST00000497377.6:n.2611_2618del
ENST00000640094.2:c.896-316_896-309del	ENSP00000491275.2:n.896-316_896-309del
ENST00000696558.1:c.1081+126_1081+133del	ENSP00000512716.1:n.1081+126_1081+133del
ENST00000696559.1:c.1012+126_1012+133del	ENSP00000512717.1:n.1012+126_1012+133del
ENST00000696560.1:c.1012+126_1012+133del	ENSP00000512718.1:n.1012+126_1012+133del
ENST00000696561.1:c.1012+126_1012+133del	ENSP00000512719.1:n.1012+126_1012+133del
ENST00000696562.1:c.1012+126_1012+133del	ENSP00000512720.1:n.1012+126_1012+133del
ENST00000412585.7:c.1012+126_1012+133del MANE Select	ENSP00000399168.2:n.1012+126_1012+133del
ENST00000640094.1:c.89-316_89-309del	ENSP00000491275.1:n.89-316_89-309del
ENST00000412585.6:c.1012+126_1012+133del	ENSP00000399168.2:n.1012+126_1012+133del
ENST00000497377.5:n.96_103del
NM_005514.6:c.1012+126_1012+133del	NP_005505.2:n.1012+126_1012+133del
XM_011514556.1:c.1045+126_1045+133del	XP_011512858.1:n.1045+126_1045+133del
XM_011514557.1:c.896-316_896-309del	XP_011512859.1:n.896-316_896-309del
XR_926175.1:n.1451+126_1451+133del
NM_005514.7:c.1012+126_1012+133del	NP_005505.2:n.1012+126_1012+133del
NM_005514.8:c.1012+126_1012+133del MANE Select	NP_005505.2:n.1012+126_1012+133del