Canonical Allele Identifier: CA2677957832

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356966-G-GGCA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356966_31356967insGCA , CM000668.2:g.31356966_31356967insGCA	GRCh38
NC_000006.11:g.31324743_31324744insGCA , CM000668.1:g.31324743_31324744insGCA	GRCh37
NC_000006.10:g.31432722_31432723insGCA	NCBI36
NG_023187.1:g.5246_5247insTGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1547-10_1547-9insTGC
ENST00000481849.6:n.1547-10_1547-9insTGC
ENST00000497377.6:n.1547-10_1547-9insTGC
ENST00000640094.2:c.74-10_74-9insTGC	ENSP00000491275.2:n.74-10_74-9insTGC
ENST00000696558.1:c.74-10_74-9insTGC	ENSP00000512716.1:n.74-10_74-9insTGC
ENST00000696559.1:c.74-10_74-9insTGC	ENSP00000512717.1:n.74-10_74-9insTGC
ENST00000696560.1:c.74-10_74-9insTGC	ENSP00000512718.1:n.74-10_74-9insTGC
ENST00000696561.1:c.74-10_74-9insTGC	ENSP00000512719.1:n.74-10_74-9insTGC
ENST00000696562.1:c.74-10_74-9insTGC	ENSP00000512720.1:n.74-10_74-9insTGC
ENST00000412585.7:c.74-10_74-9insTGC MANE Select	ENSP00000399168.2:n.74-10_74-9insTGC
ENST00000412585.6:c.74-10_74-9insTGC	ENSP00000399168.2:n.74-10_74-9insTGC
ENST00000434333.1:c.97_98insTGC	ENSP00000405931.1:p.Ser33delinsLeuPro
ENST00000498007.1:n.95-10_95-9insTGC
ENST00000603274.1:n.320_321insGCA
NM_005514.6:c.74-10_74-9insTGC	NP_005505.2:n.74-10_74-9insTGC
XM_011514556.1:c.97_98insTGC	XP_011512858.1:p.Ser33delinsLeuPro
XM_011514557.1:c.74-10_74-9insTGC	XP_011512859.1:n.74-10_74-9insTGC
XR_926175.1:n.84-10_84-9insTGC
NM_005514.7:c.74-10_74-9insTGC	NP_005505.2:n.74-10_74-9insTGC
NM_005514.8:c.74-10_74-9insTGC MANE Select	NP_005505.2:n.74-10_74-9insTGC