Canonical Allele Identifier: CA2677957928

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31357155-G-GGC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357155_31357156insGC , CM000668.2:g.31357155_31357156insGC	GRCh38
NC_000006.11:g.31324932_31324933insGC , CM000668.1:g.31324932_31324933insGC	GRCh37
NC_000006.10:g.31432911_31432912insGC	NCBI36
NG_023187.1:g.5057_5058insGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1476_1477insGC
ENST00000481849.6:n.1476_1477insGC
ENST00000497377.6:n.1476_1477insGC
ENST00000640094.2:c.3_4insGC	ENSP00000491275.2:p.Leu2AlafsTer19
ENST00000696558.1:c.3_4insGC	ENSP00000512716.1:p.Leu2AlafsTer19
ENST00000696559.1:c.3_4insGC	ENSP00000512717.1:p.Leu2AlafsTer19
ENST00000696560.1:c.3_4insGC	ENSP00000512718.1:p.Leu2AlafsTer19
ENST00000696561.1:c.3_4insGC	ENSP00000512719.1:p.Leu2AlafsTer19
ENST00000696562.1:c.3_4insGC	ENSP00000512720.1:p.Leu2AlafsTer19
ENST00000412585.7:c.3_4insGC MANE Select	ENSP00000399168.2:p.Leu2AlafsTer19
ENST00000412585.6:c.3_4insGC	ENSP00000399168.2:p.Leu2AlafsTer19
ENST00000434333.1:c.-93_-92insGC	ENSP00000405931.1:n.-93_-92insGC
ENST00000498007.1:n.24_25insGC
ENST00000603274.1:n.509_510insGC
NM_005514.6:c.3_4insGC	NP_005505.2:p.Leu2AlafsTer19
XM_011514557.1:c.3_4insGC	XP_011512859.1:p.Leu2AlafsTer19
XR_926175.1:n.13_14insGC
NM_005514.7:c.3_4insGC	NP_005505.2:p.Leu2AlafsTer19
NM_005514.8:c.3_4insGC MANE Select	NP_005505.2:p.Leu2AlafsTer19