Canonical Allele Identifier: CA2677957873

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31357072-CGA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357073_31357074del , CM000668.2:g.31357073_31357074del	GRCh38
NC_000006.11:g.31324850_31324851del , CM000668.1:g.31324850_31324851del	GRCh37
NC_000006.10:g.31432829_31432830del	NCBI36
NG_023187.1:g.5139_5140del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1546+12_1546+13del
ENST00000481849.6:n.1546+12_1546+13del
ENST00000497377.6:n.1546+12_1546+13del
ENST00000640094.2:c.73+12_73+13del	ENSP00000491275.2:n.73+12_73+13del
ENST00000696558.1:c.73+12_73+13del	ENSP00000512716.1:n.73+12_73+13del
ENST00000696559.1:c.73+12_73+13del	ENSP00000512717.1:n.73+12_73+13del
ENST00000696560.1:c.73+12_73+13del	ENSP00000512718.1:n.73+12_73+13del
ENST00000696561.1:c.73+12_73+13del	ENSP00000512719.1:n.73+12_73+13del
ENST00000696562.1:c.73+12_73+13del	ENSP00000512720.1:n.73+12_73+13del
ENST00000412585.7:c.73+12_73+13del MANE Select	ENSP00000399168.2:n.73+12_73+13del
ENST00000412585.6:c.73+12_73+13del	ENSP00000399168.2:n.73+12_73+13del
ENST00000434333.1:c.-11_-10del	ENSP00000405931.1:n.-11_-10del
ENST00000498007.1:n.94+12_94+13del
ENST00000603274.1:n.427_428del
NM_005514.6:c.73+12_73+13del	NP_005505.2:n.73+12_73+13del
XM_011514556.1:c.-11_-10del	XP_011512858.1:n.-11_-10del
XM_011514557.1:c.73+12_73+13del	XP_011512859.1:n.73+12_73+13del
XR_926175.1:n.83+12_83+13del
NM_005514.7:c.73+12_73+13del	NP_005505.2:n.73+12_73+13del
NM_005514.8:c.73+12_73+13del MANE Select	NP_005505.2:n.73+12_73+13del