Canonical Allele Identifier: CA136831278

Gene: HLA-B

Linked Data

• dbSNP Id: rs386699121
• COSMIC: COSN15648838

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354138_31354139delinsGG , CM000668.2:g.31354138_31354139delinsGG	GRCh38
NC_000006.11:g.31321915_31321916delinsGG , CM000668.1:g.31321915_31321916delinsGG	GRCh37
NC_000006.10:g.31429894_31429895delinsGG	NCBI36
NG_023187.1:g.8074_8075delinsCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3298_3299delinsCC
ENST00000481849.6:n.3258_3259delinsCC
ENST00000497377.6:n.3165_3166delinsCC
ENST00000696558.1:c.1320_1321delinsCC	ENSP00000512716.1:n.1320_1321delinsCC
ENST00000696559.1:c.*162_*163delinsCC	ENSP00000512717.1:n.*162_*163delinsCC
ENST00000696560.1:c.*162_*163delinsCC	ENSP00000512718.1:n.*162_*163delinsCC
ENST00000696561.1:c.*162_*163delinsCC	ENSP00000512719.1:n.*162_*163delinsCC
ENST00000696562.1:c.*162_*163delinsCC	ENSP00000512720.1:n.*162_*163delinsCC
ENST00000412585.7:c.*162_*163delinsCC MANE Select	ENSP00000399168.2:n.*162_*163delinsCC
ENST00000412585.6:c.*162_*163delinsCC	ENSP00000399168.2:n.*162_*163delinsCC
ENST00000481849.5:n.486_487delinsCC
ENST00000497377.5:n.650_651delinsCC
NM_005514.6:c.*162_*163delinsCC	NP_005505.2:n.*162_*163delinsCC
XM_011514556.1:c.*162_*163delinsCC	XP_011512858.1:n.*162_*163delinsCC
XM_011514557.1:c.*162_*163delinsCC	XP_011512859.1:n.*162_*163delinsCC
XR_926175.1:n.1690_1691delinsCC
NM_005514.7:c.*162_*163delinsCC	NP_005505.2:n.*162_*163delinsCC
NM_005514.8:c.*162_*163delinsCC MANE Select	NP_005505.2:n.*162_*163delinsCC