Canonical Allele Identifier: CA1619111607

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356285_31356287delinsGGT , CM000668.2:g.31356285_31356287delinsGGT	GRCh38
NC_000006.11:g.31324062_31324064delinsGGT , CM000668.1:g.31324062_31324064delinsGGT	GRCh37
NC_000006.10:g.31432041_31432043delinsGGT	NCBI36
NG_023187.1:g.5926_5928delinsACC

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1972_1974delinsACC
ENST00000481849.6:n.1972_1974delinsACC
ENST00000497377.6:n.1972_1974delinsACC
ENST00000640094.2:c.499_501delinsACC	ENSP00000491275.2:p.Thr167=
ENST00000696558.1:c.499_501delinsACC	ENSP00000512716.1:p.Thr167=
ENST00000696559.1:c.499_501delinsACC	ENSP00000512717.1:p.Thr167=
ENST00000696560.1:c.499_501delinsACC	ENSP00000512718.1:p.Thr167=
ENST00000696561.1:c.499_501delinsACC	ENSP00000512719.1:p.Thr167=
ENST00000696562.1:c.499_501delinsACC	ENSP00000512720.1:p.Thr167=
ENST00000412585.7:c.499_501delinsACC MANE Select	ENSP00000399168.2:p.Thr167=
ENST00000412585.6:c.499_501delinsACC	ENSP00000399168.2:p.Thr167=
ENST00000434333.1:c.532_534delinsACC	ENSP00000405931.1:p.Thr178=
ENST00000474381.1:n.374_376delinsACC
ENST00000498007.1:n.765_767delinsACC
NM_005514.6:c.499_501delinsACC	NP_005505.2:p.Thr167=
XM_011514556.1:c.532_534delinsACC	XP_011512858.1:p.Thr178=
XM_011514557.1:c.499_501delinsACC	XP_011512859.1:p.Thr167=
XR_926175.1:n.509_511delinsACC
NM_005514.7:c.499_501delinsACC	NP_005505.2:p.Thr167=
NM_005514.8:c.499_501delinsACC MANE Select	NP_005505.2:p.Thr167=