Canonical Allele Identifier: CA1619114077

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357052_31357053delinsGG , CM000668.2:g.31357052_31357053delinsGG	GRCh38
NC_000006.11:g.31324829_31324830delinsGG , CM000668.1:g.31324829_31324830delinsGG	GRCh37
NC_000006.10:g.31432808_31432809delinsGG	NCBI36
NG_023187.1:g.5160_5161delinsCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1546+33_1546+34delinsCC
ENST00000481849.6:n.1546+33_1546+34delinsCC
ENST00000497377.6:n.1546+33_1546+34delinsCC
ENST00000640094.2:c.73+33_73+34delinsCC	ENSP00000491275.2:n.73+33_73+34delinsCC
ENST00000696558.1:c.73+33_73+34delinsCC	ENSP00000512716.1:n.73+33_73+34delinsCC
ENST00000696559.1:c.73+33_73+34delinsCC	ENSP00000512717.1:n.73+33_73+34delinsCC
ENST00000696560.1:c.73+33_73+34delinsCC	ENSP00000512718.1:n.73+33_73+34delinsCC
ENST00000696561.1:c.73+33_73+34delinsCC	ENSP00000512719.1:n.73+33_73+34delinsCC
ENST00000696562.1:c.73+33_73+34delinsCC	ENSP00000512720.1:n.73+33_73+34delinsCC
ENST00000412585.7:c.73+33_73+34delinsCC MANE Select	ENSP00000399168.2:n.73+33_73+34delinsCC
ENST00000412585.6:c.73+33_73+34delinsCC	ENSP00000399168.2:n.73+33_73+34delinsCC
ENST00000434333.1:c.11_12delinsCC	ENSP00000405931.1:p.Ala4=
ENST00000498007.1:n.94+33_94+34delinsCC
ENST00000603274.1:n.406_407delinsGG
NM_005514.6:c.73+33_73+34delinsCC	NP_005505.2:n.73+33_73+34delinsCC
XM_011514556.1:c.11_12delinsCC	XP_011512858.1:p.Ala4=
XM_011514557.1:c.73+33_73+34delinsCC	XP_011512859.1:n.73+33_73+34delinsCC
XR_926175.1:n.83+33_83+34delinsCC
NM_005514.7:c.73+33_73+34delinsCC	NP_005505.2:n.73+33_73+34delinsCC
NM_005514.8:c.73+33_73+34delinsCC MANE Select	NP_005505.2:n.73+33_73+34delinsCC