Canonical Allele Identifier: CA136836338
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs151341199
gnomAD v2: 6-31324483-A-G
gnomAD v3: 6-31356706-A-G
gnomAD v4: 6-31356706-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356706A>G , CM000668.2:g.31356706A>G GRCh38
NC_000006.11:g.31324483A>G , CM000668.1:g.31324483A>G GRCh37
NC_000006.10:g.31432462A>G NCBI36
NG_023187.1:g.5507T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1798T>C
ENST00000481849.6:n.1798T>C
ENST00000497377.6:n.1798T>C
ENST00000640094.2:c.325T>C ENSP00000491275.2:p.Tyr109His
ENST00000696558.1:c.325T>C ENSP00000512716.1:p.Tyr109His
ENST00000696559.1:c.325T>C ENSP00000512717.1:p.Tyr109His
ENST00000696560.1:c.325T>C ENSP00000512718.1:p.Tyr109His
ENST00000696561.1:c.325T>C ENSP00000512719.1:p.Tyr109His
ENST00000696562.1:c.325T>C ENSP00000512720.1:p.Tyr109His
ENST00000412585.7:c.325T>C MANE Select ENSP00000399168.2:p.Tyr109His
ENST00000412585.6:c.325T>C ENSP00000399168.2:p.Tyr109His
ENST00000434333.1:c.358T>C ENSP00000405931.1:p.Tyr120His
ENST00000474381.1:n.200T>C
ENST00000498007.1:n.346T>C
ENST00000603274.1:n.60A>G
NM_005514.6:c.325T>C NP_005505.2:p.Tyr109His
XM_011514556.1:c.358T>C XP_011512858.1:p.Tyr120His
XM_011514557.1:c.325T>C XP_011512859.1:p.Tyr109His
XR_926175.1:n.335T>C
NM_005514.7:c.325T>C NP_005505.2:p.Tyr109His
NM_005514.8:c.325T>C MANE Select NP_005505.2:p.Tyr109His