Canonical Allele Identifier: CA1087466315
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs1766896378
gnomAD v3: 6-31355760-G-GGAAA
gnomAD v4: 6-31355760-G-GGAAA
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355762_31355765dup , CM000668.2:g.31355762_31355765dup GRCh38
NC_000006.11:g.31323539_31323542dup , CM000668.1:g.31323539_31323542dup GRCh37
NC_000006.10:g.31431518_31431521dup NCBI36
NG_023187.1:g.6449_6452dup

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.2495_2498dup
ENST00000481849.6:n.2093-172_2093-169dup
ENST00000497377.6:n.2093-172_2093-169dup
ENST00000640094.2:c.620-172_620-169dup ENSP00000491275.2:n.620-172_620-169dup
ENST00000696558.1:c.662_665dup ENSP00000512716.1:p.Asn223PhefsTer3
ENST00000696559.1:c.620-172_620-169dup ENSP00000512717.1:n.620-172_620-169dup
ENST00000696560.1:c.620-172_620-169dup ENSP00000512718.1:n.620-172_620-169dup
ENST00000696561.1:c.620-172_620-169dup ENSP00000512719.1:n.620-172_620-169dup
ENST00000696562.1:c.620-172_620-169dup ENSP00000512720.1:n.620-172_620-169dup
ENST00000412585.7:c.620-172_620-169dup MANE Select ENSP00000399168.2:n.620-172_620-169dup
ENST00000412585.6:c.620-172_620-169dup ENSP00000399168.2:n.620-172_620-169dup
ENST00000434333.1:c.653-172_653-169dup ENSP00000405931.1:n.653-172_653-169dup
ENST00000463574.1:n.39_42dup
ENST00000474381.1:n.897_900dup
ENST00000498007.1:n.886-172_886-169dup
NM_005514.6:c.620-172_620-169dup NP_005505.2:n.620-172_620-169dup
XM_011514556.1:c.653-172_653-169dup XP_011512858.1:n.653-172_653-169dup
XM_011514557.1:c.620-172_620-169dup XP_011512859.1:n.620-172_620-169dup
XR_926175.1:n.1032_1035dup
NM_005514.7:c.620-172_620-169dup NP_005505.2:n.620-172_620-169dup
NM_005514.8:c.620-172_620-169dup MANE Select NP_005505.2:n.620-172_620-169dup
Search 100 bp 5'
Search 100 bp 3'