Canonical Allele Identifier: CA2677957162

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356468-A-AGC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356469_31356470insCG , CM000668.2:g.31356469_31356470insCG	GRCh38
NC_000006.11:g.31324246_31324247insCG , CM000668.1:g.31324246_31324247insCG	GRCh37
NC_000006.10:g.31432225_31432226insCG	NCBI36
NG_023187.1:g.5744_5745insGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1817-27_1817-26insGC
ENST00000481849.6:n.1817-27_1817-26insGC
ENST00000497377.6:n.1817-27_1817-26insGC
ENST00000640094.2:c.344-27_344-26insGC	ENSP00000491275.2:n.344-27_344-26insGC
ENST00000696558.1:c.344-27_344-26insGC	ENSP00000512716.1:n.344-27_344-26insGC
ENST00000696559.1:c.344-27_344-26insGC	ENSP00000512717.1:n.344-27_344-26insGC
ENST00000696560.1:c.344-27_344-26insGC	ENSP00000512718.1:n.344-27_344-26insGC
ENST00000696561.1:c.344-27_344-26insGC	ENSP00000512719.1:n.344-27_344-26insGC
ENST00000696562.1:c.344-27_344-26insGC	ENSP00000512720.1:n.344-27_344-26insGC
ENST00000412585.7:c.344-27_344-26insGC MANE Select	ENSP00000399168.2:n.344-27_344-26insGC
ENST00000412585.6:c.344-27_344-26insGC	ENSP00000399168.2:n.344-27_344-26insGC
ENST00000434333.1:c.377-27_377-26insGC	ENSP00000405931.1:n.377-27_377-26insGC
ENST00000474381.1:n.219-27_219-26insGC
ENST00000498007.1:n.583_584insGC
NM_005514.6:c.344-27_344-26insGC	NP_005505.2:n.344-27_344-26insGC
XM_011514556.1:c.377-27_377-26insGC	XP_011512858.1:n.377-27_377-26insGC
XM_011514557.1:c.344-27_344-26insGC	XP_011512859.1:n.344-27_344-26insGC
XR_926175.1:n.354-27_354-26insGC
NM_005514.7:c.344-27_344-26insGC	NP_005505.2:n.344-27_344-26insGC
NM_005514.8:c.344-27_344-26insGC MANE Select	NP_005505.2:n.344-27_344-26insGC