Canonical Allele Identifier: CA3711727
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs9266161
gnomAD v2: 6-31324494-A-T
gnomAD v3: 6-31356717-A-T
gnomAD v4: 6-31356717-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356717A>T , CM000668.2:g.31356717A>T GRCh38
NC_000006.11:g.31324494A>T , CM000668.1:g.31324494A>T GRCh37
NC_000006.10:g.31432473A>T NCBI36
NG_023187.1:g.5496T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.1787T>A
ENST00000481849.6:n.1787T>A
ENST00000497377.6:n.1787T>A
ENST00000640094.2:c.314T>A ENSP00000491275.2:p.Leu105Gln
ENST00000696558.1:c.314T>A ENSP00000512716.1:p.Leu105Gln
ENST00000696559.1:c.314T>A ENSP00000512717.1:p.Leu105Gln
ENST00000696560.1:c.314T>A ENSP00000512718.1:p.Leu105Gln
ENST00000696561.1:c.314T>A ENSP00000512719.1:p.Leu105Gln
ENST00000696562.1:c.314T>A ENSP00000512720.1:p.Leu105Gln
ENST00000412585.7:c.314T>A MANE Select ENSP00000399168.2:p.Leu105Gln
ENST00000412585.6:c.314T>A ENSP00000399168.2:p.Leu105Gln
ENST00000434333.1:c.347T>A ENSP00000405931.1:p.Leu116Gln
ENST00000474381.1:n.189T>A
ENST00000498007.1:n.335T>A
ENST00000603274.1:n.71A>T
NM_005514.6:c.314T>A NP_005505.2:p.Leu105Gln
XM_011514556.1:c.347T>A XP_011512858.1:p.Leu116Gln
XM_011514557.1:c.314T>A XP_011512859.1:p.Leu105Gln
XR_926175.1:n.324T>A
NM_005514.7:c.314T>A NP_005505.2:p.Leu105Gln
NM_005514.8:c.314T>A MANE Select NP_005505.2:p.Leu105Gln