Canonical Allele Identifier: CA2677957878

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31357074-A-ACC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357076_31357077dup , CM000668.2:g.31357076_31357077dup	GRCh38
NC_000006.11:g.31324853_31324854dup , CM000668.1:g.31324853_31324854dup	GRCh37
NC_000006.10:g.31432832_31432833dup	NCBI36
NG_023187.1:g.5137_5138dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1546+10_1546+11dup
ENST00000481849.6:n.1546+10_1546+11dup
ENST00000497377.6:n.1546+10_1546+11dup
ENST00000640094.2:c.73+10_73+11dup	ENSP00000491275.2:n.73+10_73+11dup
ENST00000696558.1:c.73+10_73+11dup	ENSP00000512716.1:n.73+10_73+11dup
ENST00000696559.1:c.73+10_73+11dup	ENSP00000512717.1:n.73+10_73+11dup
ENST00000696560.1:c.73+10_73+11dup	ENSP00000512718.1:n.73+10_73+11dup
ENST00000696561.1:c.73+10_73+11dup	ENSP00000512719.1:n.73+10_73+11dup
ENST00000696562.1:c.73+10_73+11dup	ENSP00000512720.1:n.73+10_73+11dup
ENST00000412585.7:c.73+10_73+11dup MANE Select	ENSP00000399168.2:n.73+10_73+11dup
ENST00000412585.6:c.73+10_73+11dup	ENSP00000399168.2:n.73+10_73+11dup
ENST00000434333.1:c.-13_-12dup	ENSP00000405931.1:n.-13_-12dup
ENST00000498007.1:n.94+10_94+11dup
ENST00000603274.1:n.430_431dup
NM_005514.6:c.73+10_73+11dup	NP_005505.2:n.73+10_73+11dup
XM_011514556.1:c.-13_-12dup	XP_011512858.1:n.-13_-12dup
XM_011514557.1:c.73+10_73+11dup	XP_011512859.1:n.73+10_73+11dup
XR_926175.1:n.83+10_83+11dup
NM_005514.7:c.73+10_73+11dup	NP_005505.2:n.73+10_73+11dup
NM_005514.8:c.73+10_73+11dup MANE Select	NP_005505.2:n.73+10_73+11dup