Canonical Allele Identifier: CA2677953885

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31354434-C-CACTTCAGCTCGACACACGCGAAACAT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354434_31354435insACTTCAGCTCGACACACGCGAAACAT , CM000668.2:g.31354434_31354435insACTTCAGCTCGACACACGCGAAACAT	GRCh38
NC_000006.11:g.31322211_31322212insACTTCAGCTCGACACACGCGAAACAT , CM000668.1:g.31322211_31322212insACTTCAGCTCGACACACGCGAAACAT	GRCh37
NC_000006.10:g.31430190_31430191insACTTCAGCTCGACACACGCGAAACAT	NCBI36
NG_023187.1:g.7778_7779insATGTTTCGCGTGTGTCGAGCTGAAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3140+44_3140+45insATGTTTCGCGTGTGTCGAGCTGAAGT
ENST00000481849.6:n.3100+44_3100+45insATGTTTCGCGTGTGTCGAGCTGAAGT
ENST00000497377.6:n.3007+44_3007+45insATGTTTCGCGTGTGTCGAGCTGAAGT
ENST00000696558.1:c.1162+44_1162+45insATGTTTCGCGTGTGTCGAGCTGAAGT	ENSP00000512716.1:n.1162+44_1162+45insATGTTTCGCGTGTGTCGAGCTGA...
ENST00000696559.1:c.*4+44_*4+45insATGTTTCGCGTGTGTCGAGCTGAAGT	ENSP00000512717.1:n.*4+44_*4+45insATGTTTCGCGTGTGTCGAGCTGAAGT
ENST00000696560.1:c.*4+44_*4+45insATGTTTCGCGTGTGTCGAGCTGAAGT	ENSP00000512718.1:n.*4+44_*4+45insATGTTTCGCGTGTGTCGAGCTGAAGT
ENST00000696561.1:c.*4+44_*4+45insATGTTTCGCGTGTGTCGAGCTGAAGT	ENSP00000512719.1:n.*4+44_*4+45insATGTTTCGCGTGTGTCGAGCTGAAGT
ENST00000696562.1:c.*4+44_*4+45insATGTTTCGCGTGTGTCGAGCTGAAGT	ENSP00000512720.1:n.*4+44_*4+45insATGTTTCGCGTGTGTCGAGCTGAAGT
ENST00000412585.7:c.*4+44_*4+45insATGTTTCGCGTGTGTCGAGCTGAAGT MANE Select	ENSP00000399168.2:n.*4+44_*4+45insATGTTTCGCGTGTGTCGAGCTGAAGT
ENST00000412585.6:c.*4+44_*4+45insATGTTTCGCGTGTGTCGAGCTGAAGT	ENSP00000399168.2:n.*4+44_*4+45insATGTTTCGCGTGTGTCGAGCTGAAGT
ENST00000481849.5:n.328+44_328+45insATGTTTCGCGTGTGTCGAGCTGAAGT
ENST00000497377.5:n.492+44_492+45insATGTTTCGCGTGTGTCGAGCTGAAGT
NM_005514.6:c.*4+44_*4+45insATGTTTCGCGTGTGTCGAGCTGAAGT	NP_005505.2:n.*4+44_*4+45insATGTTTCGCGTGTGTCGAGCTGAAGT
XM_011514556.1:c.*4+44_*4+45insATGTTTCGCGTGTGTCGAGCTGAAGT	XP_011512858.1:n.*4+44_*4+45insATGTTTCGCGTGTGTCGAGCTGAAGT
XM_011514557.1:c.*4+44_*4+45insATGTTTCGCGTGTGTCGAGCTGAAGT	XP_011512859.1:n.*4+44_*4+45insATGTTTCGCGTGTGTCGAGCTGAAGT
XR_926175.1:n.1532+44_1532+45insATGTTTCGCGTGTGTCGAGCTGAAGT
NM_005514.7:c.*4+44_*4+45insATGTTTCGCGTGTGTCGAGCTGAAGT	NP_005505.2:n.*4+44_*4+45insATGTTTCGCGTGTGTCGAGCTGAAGT
NM_005514.8:c.*4+44_*4+45insATGTTTCGCGTGTGTCGAGCTGAAGT MANE Select	NP_005505.2:n.*4+44_*4+45insATGTTTCGCGTGTGTCGAGCTGAAGT