Canonical Allele Identifier: CA2711310462

Gene: HLA-B

Linked Data

• dbSNP Id: rs2113732954

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354670_31354671insCTCTTCCTCCTACACATCACAGTAGCGACCACAGCTCC , CM000668.2:g.31354670_31354671insCTCTTCCTCCTACACATCACAGTAGCGACCACAGCTCC	GRCh38
NC_000006.11:g.31322447_31322448insCTCTTCCTCCTACACATCACAGTAGCGACCACAGCTCC , CM000668.1:g.31322447_31322448insCTCTTCCTCCTACACATCACAGTAGCGACCACAGCTCC	GRCh37
NC_000006.10:g.31430426_31430427insCTCTTCCTCCTACACATCACAGTAGCGACCACAGCTCC	NCBI36
NG_023187.1:g.7542_7543insGGAGCTGTGGTCGCTACTGTGATGTGTAGGAGGAAGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3060-6_3060-5insGGAGCTGTGGTCGCTACTGTGATGTGTAGGAGGAAGAG
ENST00000481849.6:n.3014_3015insGGAGCTGTGGTCGCTACTGTGATGTGTAGGAGGAAGAG
ENST00000497377.6:n.2921_2922insGGAGCTGTGGTCGCTACTGTGATGTGTAGGAGGAAGAG
ENST00000640094.2:c.896-6_896-5insGGAGCTGTGGTCGCTACTGTGATGTGTAGGAGGAAGAG	ENSP00000491275.2:n.896-6_896-5insGGAGCTGTGGTCGCTACTGTGATGTGT...
ENST00000696558.1:c.1082-6_1082-5insGGAGCTGTGGTCGCTACTGTGATGTGTAGGAGGAAGAG	ENSP00000512716.1:n.1082-6_1082-5insGGAGCTGTGGTCGCTACTGTGATGT...
ENST00000696559.1:c.1013-6_1013-5insGGAGCTGTGGTCGCTACTGTGATGTGTAGGAGGAAGAG	ENSP00000512717.1:n.1013-6_1013-5insGGAGCTGTGGTCGCTACTGTGATGT...
ENST00000696560.1:c.1013-6_1013-5insGGAGCTGTGGTCGCTACTGTGATGTGTAGGAGGAAGAG	ENSP00000512718.1:n.1013-6_1013-5insGGAGCTGTGGTCGCTACTGTGATGT...
ENST00000696561.1:c.1013-6_1013-5insGGAGCTGTGGTCGCTACTGTGATGTGTAGGAGGAAGAG	ENSP00000512719.1:n.1013-6_1013-5insGGAGCTGTGGTCGCTACTGTGATGT...
ENST00000696562.1:c.1013-6_1013-5insGGAGCTGTGGTCGCTACTGTGATGTGTAGGAGGAAGAG	ENSP00000512720.1:n.1013-6_1013-5insGGAGCTGTGGTCGCTACTGTGATGT...
ENST00000412585.7:c.1013-6_1013-5insGGAGCTGTGGTCGCTACTGTGATGTGTAGGAGGAAGAG MANE Select	ENSP00000399168.2:n.1013-6_1013-5insGGAGCTGTGGTCGCTACTGTGATGT...
ENST00000640094.1:c.89-6_89-5insGGAGCTGTGGTCGCTACTGTGATGTGTAGGAGGAAGAG	ENSP00000491275.1:n.89-6_89-5insGGAGCTGTGGTCGCTACTGTGATGTGTAG...
ENST00000412585.6:c.1013-6_1013-5insGGAGCTGTGGTCGCTACTGTGATGTGTAGGAGGAAGAG	ENSP00000399168.2:n.1013-6_1013-5insGGAGCTGTGGTCGCTACTGTGATGT...
ENST00000481849.5:n.136_137insGGAGCTGTGGTCGCTACTGTGATGTGTAGGAGGAAGAG
ENST00000497377.5:n.406_407insGGAGCTGTGGTCGCTACTGTGATGTGTAGGAGGAAGAG
NM_005514.6:c.1013-6_1013-5insGGAGCTGTGGTCGCTACTGTGATGTGTAGGAGGAAGAG	NP_005505.2:n.1013-6_1013-5insGGAGCTGTGGTCGCTACTGTGATGTGTAGGA...
XM_011514556.1:c.1046-6_1046-5insGGAGCTGTGGTCGCTACTGTGATGTGTAGGAGGAAGAG	XP_011512858.1:n.1046-6_1046-5insGGAGCTGTGGTCGCTACTGTGATGTGTA...
XM_011514557.1:c.896-6_896-5insGGAGCTGTGGTCGCTACTGTGATGTGTAGGAGGAAGAG	XP_011512859.1:n.896-6_896-5insGGAGCTGTGGTCGCTACTGTGATGTGTAGG...
XR_926175.1:n.1452-6_1452-5insGGAGCTGTGGTCGCTACTGTGATGTGTAGGAGGAAGAG
NM_005514.7:c.1013-6_1013-5insGGAGCTGTGGTCGCTACTGTGATGTGTAGGAGGAAGAG	NP_005505.2:n.1013-6_1013-5insGGAGCTGTGGTCGCTACTGTGATGTGTAGGA...
NM_005514.8:c.1013-6_1013-5insGGAGCTGTGGTCGCTACTGTGATGTGTAGGAGGAAGAG MANE Select	NP_005505.2:n.1013-6_1013-5insGGAGCTGTGGTCGCTACTGTGATGTGTAGGA...