Canonical Allele Identifier: CA2677953093

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31354140-G-GGA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354141_31354142insAG , CM000668.2:g.31354141_31354142insAG	GRCh38
NC_000006.11:g.31321918_31321919insAG , CM000668.1:g.31321918_31321919insAG	GRCh37
NC_000006.10:g.31429897_31429898insAG	NCBI36
NG_023187.1:g.8072_8073insTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3296_3297insTC
ENST00000481849.6:n.3256_3257insTC
ENST00000497377.6:n.3163_3164insTC
ENST00000696558.1:c.1318_1319insTC	ENSP00000512716.1:n.1318_1319insTC
ENST00000696559.1:c.*160_*161insTC	ENSP00000512717.1:n.*160_*161insTC
ENST00000696560.1:c.*160_*161insTC	ENSP00000512718.1:n.*160_*161insTC
ENST00000696561.1:c.*160_*161insTC	ENSP00000512719.1:n.*160_*161insTC
ENST00000696562.1:c.*160_*161insTC	ENSP00000512720.1:n.*160_*161insTC
ENST00000412585.7:c.*160_*161insTC MANE Select	ENSP00000399168.2:n.*160_*161insTC
ENST00000412585.6:c.*160_*161insTC	ENSP00000399168.2:n.*160_*161insTC
ENST00000481849.5:n.484_485insTC
ENST00000497377.5:n.648_649insTC
NM_005514.6:c.*160_*161insTC	NP_005505.2:n.*160_*161insTC
XM_011514556.1:c.*160_*161insTC	XP_011512858.1:n.*160_*161insTC
XM_011514557.1:c.*160_*161insTC	XP_011512859.1:n.*160_*161insTC
XR_926175.1:n.1688_1689insTC
NM_005514.7:c.*160_*161insTC	NP_005505.2:n.*160_*161insTC
NM_005514.8:c.*160_*161insTC MANE Select	NP_005505.2:n.*160_*161insTC