Canonical Allele Identifier: CA1619116504
Gene: HLA-B HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31354137_31354139delinsCAA , CM000668.2:g.31354137_31354139delinsCAA GRCh38
NC_000006.11:g.31321914_31321916delinsCAA , CM000668.1:g.31321914_31321916delinsCAA GRCh37
NC_000006.10:g.31429893_31429895delinsCAA NCBI36
NG_023187.1:g.8074_8076delinsTTG

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.3298_3300delinsTTG
ENST00000481849.6:n.3258_3260delinsTTG
ENST00000497377.6:n.3165_3167delinsTTG
ENST00000696558.1:c.1320_1322delinsTTG ENSP00000512716.1:n.1320_1322delinsTTG
ENST00000696559.1:c.*162_*164delinsTTG ENSP00000512717.1:n.*162_*164delinsTTG
ENST00000696560.1:c.*162_*164delinsTTG ENSP00000512718.1:n.*162_*164delinsTTG
ENST00000696561.1:c.*162_*164delinsTTG ENSP00000512719.1:n.*162_*164delinsTTG
ENST00000696562.1:c.*162_*164delinsTTG ENSP00000512720.1:n.*162_*164delinsTTG
ENST00000412585.7:c.*162_*164delinsTTG MANE Select ENSP00000399168.2:n.*162_*164delinsTTG
ENST00000412585.6:c.*162_*164delinsTTG ENSP00000399168.2:n.*162_*164delinsTTG
ENST00000481849.5:n.486_488delinsTTG
ENST00000497377.5:n.650_652delinsTTG
NM_005514.6:c.*162_*164delinsTTG NP_005505.2:n.*162_*164delinsTTG
XM_011514556.1:c.*162_*164delinsTTG XP_011512858.1:n.*162_*164delinsTTG
XM_011514557.1:c.*162_*164delinsTTG XP_011512859.1:n.*162_*164delinsTTG
XR_926175.1:n.1690_1692delinsTTG
NM_005514.7:c.*162_*164delinsTTG NP_005505.2:n.*162_*164delinsTTG
NM_005514.8:c.*162_*164delinsTTG MANE Select NP_005505.2:n.*162_*164delinsTTG
Search 100 bp 5'
Search 100 bp 3'