Canonical Allele Identifier: CA2677957591
Gene: HLA-B HGNC NCBI

Linked Data

gnomAD v4: 6-31356654-G-GGGT
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356654_31356655insGGT , CM000668.2:g.31356654_31356655insGGT GRCh38
NC_000006.11:g.31324431_31324432insGGT , CM000668.1:g.31324431_31324432insGGT GRCh37
NC_000006.10:g.31432410_31432411insGGT NCBI36
NG_023187.1:g.5558_5559insACC

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.1816+33_1816+34insACC
ENST00000481849.6:n.1816+33_1816+34insACC
ENST00000497377.6:n.1816+33_1816+34insACC
ENST00000640094.2:c.343+33_343+34insACC ENSP00000491275.2:n.343+33_343+34insACC
ENST00000696558.1:c.343+33_343+34insACC ENSP00000512716.1:n.343+33_343+34insACC
ENST00000696559.1:c.343+33_343+34insACC ENSP00000512717.1:n.343+33_343+34insACC
ENST00000696560.1:c.343+33_343+34insACC ENSP00000512718.1:n.343+33_343+34insACC
ENST00000696561.1:c.343+33_343+34insACC ENSP00000512719.1:n.343+33_343+34insACC
ENST00000696562.1:c.343+33_343+34insACC ENSP00000512720.1:n.343+33_343+34insACC
ENST00000412585.7:c.343+33_343+34insACC MANE Select ENSP00000399168.2:n.343+33_343+34insACC
ENST00000412585.6:c.343+33_343+34insACC ENSP00000399168.2:n.343+33_343+34insACC
ENST00000434333.1:c.376+33_376+34insACC ENSP00000405931.1:n.376+33_376+34insACC
ENST00000474381.1:n.218+33_218+34insACC
ENST00000498007.1:n.397_398insACC
ENST00000603274.1:n.8_9insGGT
NM_005514.6:c.343+33_343+34insACC NP_005505.2:n.343+33_343+34insACC
XM_011514556.1:c.376+33_376+34insACC XP_011512858.1:n.376+33_376+34insACC
XM_011514557.1:c.343+33_343+34insACC XP_011512859.1:n.343+33_343+34insACC
XR_926175.1:n.353+33_353+34insACC
NM_005514.7:c.343+33_343+34insACC NP_005505.2:n.343+33_343+34insACC
NM_005514.8:c.343+33_343+34insACC MANE Select NP_005505.2:n.343+33_343+34insACC
Search 100 bp 5'
Search 100 bp 3'