Canonical Allele Identifier: CA2711310430
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs2113732954

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31354670_31354671insCTCTTCCTCCTACACATCACAGTAGCGACCACA , CM000668.2:g.31354670_31354671insCTCTTCCTCCTACACATCACAGTAGCGACCACA GRCh38
NC_000006.11:g.31322447_31322448insCTCTTCCTCCTACACATCACAGTAGCGACCACA , CM000668.1:g.31322447_31322448insCTCTTCCTCCTACACATCACAGTAGCGACCACA GRCh37
NC_000006.10:g.31430426_31430427insCTCTTCCTCCTACACATCACAGTAGCGACCACA NCBI36
NG_023187.1:g.7542_7543insTGTGGTCGCTACTGTGATGTGTAGGAGGAAGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.3060-6_3060-5insTGTGGTCGCTACTGTGATGTGTAGGAGGAAGAG
ENST00000481849.6:n.3014_3015insTGTGGTCGCTACTGTGATGTGTAGGAGGAAGAG
ENST00000497377.6:n.2921_2922insTGTGGTCGCTACTGTGATGTGTAGGAGGAAGAG
ENST00000640094.2:c.896-6_896-5insTGTGGTCGCTACTGTGATGTGTAGGAGGAAGAG ENSP00000491275.2:n.896-6_896-5insTGTGGTCGCTACTGTGATGTGTAGGAG...
ENST00000696558.1:c.1082-6_1082-5insTGTGGTCGCTACTGTGATGTGTAGGAGGAAGAG ENSP00000512716.1:n.1082-6_1082-5insTGTGGTCGCTACTGTGATGTGTAGG...
ENST00000696559.1:c.1013-6_1013-5insTGTGGTCGCTACTGTGATGTGTAGGAGGAAGAG ENSP00000512717.1:n.1013-6_1013-5insTGTGGTCGCTACTGTGATGTGTAGG...
ENST00000696560.1:c.1013-6_1013-5insTGTGGTCGCTACTGTGATGTGTAGGAGGAAGAG ENSP00000512718.1:n.1013-6_1013-5insTGTGGTCGCTACTGTGATGTGTAGG...
ENST00000696561.1:c.1013-6_1013-5insTGTGGTCGCTACTGTGATGTGTAGGAGGAAGAG ENSP00000512719.1:n.1013-6_1013-5insTGTGGTCGCTACTGTGATGTGTAGG...
ENST00000696562.1:c.1013-6_1013-5insTGTGGTCGCTACTGTGATGTGTAGGAGGAAGAG ENSP00000512720.1:n.1013-6_1013-5insTGTGGTCGCTACTGTGATGTGTAGG...
ENST00000412585.7:c.1013-6_1013-5insTGTGGTCGCTACTGTGATGTGTAGGAGGAAGAG MANE Select ENSP00000399168.2:n.1013-6_1013-5insTGTGGTCGCTACTGTGATGTGTAGG...
ENST00000640094.1:c.89-6_89-5insTGTGGTCGCTACTGTGATGTGTAGGAGGAAGAG ENSP00000491275.1:n.89-6_89-5insTGTGGTCGCTACTGTGATGTGTAGGAGGA...
ENST00000412585.6:c.1013-6_1013-5insTGTGGTCGCTACTGTGATGTGTAGGAGGAAGAG ENSP00000399168.2:n.1013-6_1013-5insTGTGGTCGCTACTGTGATGTGTAGG...
ENST00000481849.5:n.136_137insTGTGGTCGCTACTGTGATGTGTAGGAGGAAGAG
ENST00000497377.5:n.406_407insTGTGGTCGCTACTGTGATGTGTAGGAGGAAGAG
NM_005514.6:c.1013-6_1013-5insTGTGGTCGCTACTGTGATGTGTAGGAGGAAGAG NP_005505.2:n.1013-6_1013-5insTGTGGTCGCTACTGTGATGTGTAGGAGGAAG...
XM_011514556.1:c.1046-6_1046-5insTGTGGTCGCTACTGTGATGTGTAGGAGGAAGAG XP_011512858.1:n.1046-6_1046-5insTGTGGTCGCTACTGTGATGTGTAGGAGG...
XM_011514557.1:c.896-6_896-5insTGTGGTCGCTACTGTGATGTGTAGGAGGAAGAG XP_011512859.1:n.896-6_896-5insTGTGGTCGCTACTGTGATGTGTAGGAGGAA...
XR_926175.1:n.1452-6_1452-5insTGTGGTCGCTACTGTGATGTGTAGGAGGAAGAG
NM_005514.7:c.1013-6_1013-5insTGTGGTCGCTACTGTGATGTGTAGGAGGAAGAG NP_005505.2:n.1013-6_1013-5insTGTGGTCGCTACTGTGATGTGTAGGAGGAAG...
NM_005514.8:c.1013-6_1013-5insTGTGGTCGCTACTGTGATGTGTAGGAGGAAGAG MANE Select NP_005505.2:n.1013-6_1013-5insTGTGGTCGCTACTGTGATGTGTAGGAGGAAG...