Canonical Allele Identifier: CA2677957590
Gene: HLA-B HGNC NCBI

Linked Data

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

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356654_31356655insGGA , CM000668.2:g.31356654_31356655insGGA GRCh38
NC_000006.11:g.31324431_31324432insGGA , CM000668.1:g.31324431_31324432insGGA GRCh37
NC_000006.10:g.31432410_31432411insGGA NCBI36
NG_023187.1:g.5558_5559insTCC

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.1816+33_1816+34insTCC
ENST00000481849.6:n.1816+33_1816+34insTCC
ENST00000497377.6:n.1816+33_1816+34insTCC
ENST00000640094.2:c.343+33_343+34insTCC ENSP00000491275.2:n.343+33_343+34insTCC
ENST00000696558.1:c.343+33_343+34insTCC ENSP00000512716.1:n.343+33_343+34insTCC
ENST00000696559.1:c.343+33_343+34insTCC ENSP00000512717.1:n.343+33_343+34insTCC
ENST00000696560.1:c.343+33_343+34insTCC ENSP00000512718.1:n.343+33_343+34insTCC
ENST00000696561.1:c.343+33_343+34insTCC ENSP00000512719.1:n.343+33_343+34insTCC
ENST00000696562.1:c.343+33_343+34insTCC ENSP00000512720.1:n.343+33_343+34insTCC
ENST00000412585.7:c.343+33_343+34insTCC MANE Select ENSP00000399168.2:n.343+33_343+34insTCC
ENST00000412585.6:c.343+33_343+34insTCC ENSP00000399168.2:n.343+33_343+34insTCC
ENST00000434333.1:c.376+33_376+34insTCC ENSP00000405931.1:n.376+33_376+34insTCC
ENST00000474381.1:n.218+33_218+34insTCC
ENST00000498007.1:n.397_398insTCC
ENST00000603274.1:n.8_9insGGA
NM_005514.6:c.343+33_343+34insTCC NP_005505.2:n.343+33_343+34insTCC
XM_011514556.1:c.376+33_376+34insTCC XP_011512858.1:n.376+33_376+34insTCC
XM_011514557.1:c.343+33_343+34insTCC XP_011512859.1:n.343+33_343+34insTCC
XR_926175.1:n.353+33_353+34insTCC
NM_005514.7:c.343+33_343+34insTCC NP_005505.2:n.343+33_343+34insTCC
NM_005514.8:c.343+33_343+34insTCC MANE Select NP_005505.2:n.343+33_343+34insTCC
Search 100 bp 5'
Search 100 bp 3'