Canonical Allele Identifier: CA136836652
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs1050502
gnomAD v3: 6-31356890-G-C
gnomAD v4: 6-31356890-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356890G>C , CM000668.2:g.31356890G>C GRCh38
NC_000006.11:g.31324667G>C , CM000668.1:g.31324667G>C GRCh37
NC_000006.10:g.31432646G>C NCBI36
NG_023187.1:g.5323C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.1614C>G
ENST00000481849.6:n.1614C>G
ENST00000497377.6:n.1614C>G
ENST00000640094.2:c.141C>G ENSP00000491275.2:p.Ile47Met
ENST00000696558.1:c.141C>G ENSP00000512716.1:p.Ile47Met
ENST00000696559.1:c.141C>G ENSP00000512717.1:p.Ile47Met
ENST00000696560.1:c.141C>G ENSP00000512718.1:p.Ile47Met
ENST00000696561.1:c.141C>G ENSP00000512719.1:p.Ile47Met
ENST00000696562.1:c.141C>G ENSP00000512720.1:p.Ile47Met
ENST00000412585.7:c.141C>G MANE Select ENSP00000399168.2:p.Ile47Met
ENST00000412585.6:c.141C>G ENSP00000399168.2:p.Ile47Met
ENST00000434333.1:c.174C>G ENSP00000405931.1:p.Ile58Met
ENST00000474381.1:n.16C>G
ENST00000498007.1:n.162C>G
ENST00000603274.1:n.244G>C
NM_005514.6:c.141C>G NP_005505.2:p.Ile47Met
XM_011514556.1:c.174C>G XP_011512858.1:p.Ile58Met
XM_011514557.1:c.141C>G XP_011512859.1:p.Ile47Met
XR_926175.1:n.151C>G
NM_005514.7:c.141C>G NP_005505.2:p.Ile47Met
NM_005514.8:c.141C>G MANE Select NP_005505.2:p.Ile47Met