Canonical Allele Identifier: CA15453463
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs1055821
gnomAD v2: 6-31321919-G-T
gnomAD v3: 6-31354142-G-T
gnomAD v4: 6-31354142-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31354142G>T , CM000668.2:g.31354142G>T GRCh38
NC_000006.11:g.31321919G>T , CM000668.1:g.31321919G>T GRCh37
NC_000006.10:g.31429898G>T NCBI36
NG_023187.1:g.8071C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.3295C>A
ENST00000481849.6:n.3255C>A
ENST00000497377.6:n.3162C>A
ENST00000696558.1:c.1317C>A ENSP00000512716.1:n.1317C>A
ENST00000696559.1:c.*159C>A ENSP00000512717.1:n.*159C>A
ENST00000696560.1:c.*159C>A ENSP00000512718.1:n.*159C>A
ENST00000696561.1:c.*159C>A ENSP00000512719.1:n.*159C>A
ENST00000696562.1:c.*159C>A ENSP00000512720.1:n.*159C>A
ENST00000412585.7:c.*159C>A MANE Select ENSP00000399168.2:n.*159C>A
ENST00000412585.6:c.*159C>A ENSP00000399168.2:n.*159C>A
ENST00000481849.5:n.483C>A
ENST00000497377.5:n.647C>A
NM_005514.6:c.*159C>A NP_005505.2:n.*159C>A
XM_011514556.1:c.*159C>A XP_011512858.1:n.*159C>A
XM_011514557.1:c.*159C>A XP_011512859.1:n.*159C>A
XR_926175.1:n.1687C>A
NM_005514.7:c.*159C>A NP_005505.2:n.*159C>A
NM_005514.8:c.*159C>A MANE Select NP_005505.2:n.*159C>A