Canonical Allele Identifier: CA2677956567
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356185_31356186insAC , CM000668.2:g.31356185_31356186insAC GRCh38
NC_000006.11:g.31323962_31323963insAC , CM000668.1:g.31323962_31323963insAC GRCh37
NC_000006.10:g.31431941_31431942insAC NCBI36
NG_023187.1:g.6028_6029insTG

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.2074_2075insTG
ENST00000481849.6:n.2074_2075insTG
ENST00000497377.6:n.2074_2075insTG
ENST00000640094.2:c.601_602insTG ENSP00000491275.2:p.Asp201ValfsTer14
ENST00000696558.1:c.601_602insTG ENSP00000512716.1:p.Asp201ValfsTer?
ENST00000696559.1:c.601_602insTG ENSP00000512717.1:p.Asp201ValfsTer14
ENST00000696560.1:c.601_602insTG ENSP00000512718.1:p.Asp201ValfsTer14
ENST00000696561.1:c.601_602insTG ENSP00000512719.1:p.Asp201ValfsTer14
ENST00000696562.1:c.601_602insTG ENSP00000512720.1:p.Asp201ValfsTer14
ENST00000412585.7:c.601_602insTG MANE Select ENSP00000399168.2:p.Asp201ValfsTer14
ENST00000412585.6:c.601_602insTG ENSP00000399168.2:p.Asp201ValfsTer14
ENST00000434333.1:c.634_635insTG ENSP00000405931.1:p.Asp212ValfsTer14
ENST00000474381.1:n.476_477insTG
ENST00000498007.1:n.867_868insTG
NM_005514.6:c.601_602insTG NP_005505.2:p.Asp201ValfsTer14
XM_011514556.1:c.634_635insTG XP_011512858.1:p.Asp212ValfsTer14
XM_011514557.1:c.601_602insTG XP_011512859.1:p.Asp201ValfsTer14
XR_926175.1:n.611_612insTG
NM_005514.7:c.601_602insTG NP_005505.2:p.Asp201ValfsTer14
NM_005514.8:c.601_602insTG MANE Select NP_005505.2:p.Asp201ValfsTer14