Canonical Allele Identifier: CA2677957786

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356886-C-CGGT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356886_31356887insGGT , CM000668.2:g.31356886_31356887insGGT	GRCh38
NC_000006.11:g.31324663_31324664insGGT , CM000668.1:g.31324663_31324664insGGT	GRCh37
NC_000006.10:g.31432642_31432643insGGT	NCBI36
NG_023187.1:g.5326_5327insACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1617_1618insACC
ENST00000481849.6:n.1617_1618insACC
ENST00000497377.6:n.1617_1618insACC
ENST00000640094.2:c.144_145insACC	ENSP00000491275.2:p.Ser48_Val49insThr
ENST00000696558.1:c.144_145insACC	ENSP00000512716.1:p.Ser48_Val49insThr
ENST00000696559.1:c.144_145insACC	ENSP00000512717.1:p.Ser48_Val49insThr
ENST00000696560.1:c.144_145insACC	ENSP00000512718.1:p.Ser48_Val49insThr
ENST00000696561.1:c.144_145insACC	ENSP00000512719.1:p.Ser48_Val49insThr
ENST00000696562.1:c.144_145insACC	ENSP00000512720.1:p.Ser48_Val49insThr
ENST00000412585.7:c.144_145insACC MANE Select	ENSP00000399168.2:p.Ser48_Val49insThr
ENST00000412585.6:c.144_145insACC	ENSP00000399168.2:p.Ser48_Val49insThr
ENST00000434333.1:c.177_178insACC	ENSP00000405931.1:p.Ser59_Val60insThr
ENST00000474381.1:n.19_20insACC
ENST00000498007.1:n.165_166insACC
ENST00000603274.1:n.240_241insGGT
NM_005514.6:c.144_145insACC	NP_005505.2:p.Ser48_Val49insThr
XM_011514556.1:c.177_178insACC	XP_011512858.1:p.Ser59_Val60insThr
XM_011514557.1:c.144_145insACC	XP_011512859.1:p.Ser48_Val49insThr
XR_926175.1:n.154_155insACC
NM_005514.7:c.144_145insACC	NP_005505.2:p.Ser48_Val49insThr
NM_005514.8:c.144_145insACC MANE Select	NP_005505.2:p.Ser48_Val49insThr