Canonical Allele Identifier: CA2677953097

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31354141-G-GGC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354142_31354143insCG , CM000668.2:g.31354142_31354143insCG	GRCh38
NC_000006.11:g.31321919_31321920insCG , CM000668.1:g.31321919_31321920insCG	GRCh37
NC_000006.10:g.31429898_31429899insCG	NCBI36
NG_023187.1:g.8071_8072insGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3295_3296insGC
ENST00000481849.6:n.3255_3256insGC
ENST00000497377.6:n.3162_3163insGC
ENST00000696558.1:c.1317_1318insGC	ENSP00000512716.1:n.1317_1318insGC
ENST00000696559.1:c.*159_*160insGC	ENSP00000512717.1:n.*159_*160insGC
ENST00000696560.1:c.*159_*160insGC	ENSP00000512718.1:n.*159_*160insGC
ENST00000696561.1:c.*159_*160insGC	ENSP00000512719.1:n.*159_*160insGC
ENST00000696562.1:c.*159_*160insGC	ENSP00000512720.1:n.*159_*160insGC
ENST00000412585.7:c.*159_*160insGC MANE Select	ENSP00000399168.2:n.*159_*160insGC
ENST00000412585.6:c.*159_*160insGC	ENSP00000399168.2:n.*159_*160insGC
ENST00000481849.5:n.483_484insGC
ENST00000497377.5:n.647_648insGC
NM_005514.6:c.*159_*160insGC	NP_005505.2:n.*159_*160insGC
XM_011514556.1:c.*159_*160insGC	XP_011512858.1:n.*159_*160insGC
XM_011514557.1:c.*159_*160insGC	XP_011512859.1:n.*159_*160insGC
XR_926175.1:n.1687_1688insGC
NM_005514.7:c.*159_*160insGC	NP_005505.2:n.*159_*160insGC
NM_005514.8:c.*159_*160insGC MANE Select	NP_005505.2:n.*159_*160insGC