Canonical Allele Identifier: CA1619113755
Gene: HLA-B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356949A= , CM000668.2:g.31356949A= GRCh38
NC_000006.11:g.31324726A= , CM000668.1:g.31324726A= GRCh37
NC_000006.10:g.31432705A= NCBI36
NG_023187.1:g.5264T=

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.1555T=
ENST00000481849.6:n.1555T=
ENST00000497377.6:n.1555T=
ENST00000640094.2:c.82T= ENSP00000491275.2:p.Ser28=
ENST00000696558.1:c.82T= ENSP00000512716.1:p.Ser28=
ENST00000696559.1:c.82T= ENSP00000512717.1:p.Ser28=
ENST00000696560.1:c.82T= ENSP00000512718.1:p.Ser28=
ENST00000696561.1:c.82T= ENSP00000512719.1:p.Ser28=
ENST00000696562.1:c.82T= ENSP00000512720.1:p.Ser28=
ENST00000412585.7:c.82T= MANE Select ENSP00000399168.2:p.Ser28=
ENST00000412585.6:c.82T= ENSP00000399168.2:p.Ser28=
ENST00000434333.1:c.115T= ENSP00000405931.1:p.Ser39=
ENST00000498007.1:n.103T=
ENST00000603274.1:n.303A=
NM_005514.6:c.82T= NP_005505.2:p.Ser28=
XM_011514556.1:c.115T= XP_011512858.1:p.Ser39=
XM_011514557.1:c.82T= XP_011512859.1:p.Ser28=
XR_926175.1:n.92T=
NM_005514.7:c.82T= NP_005505.2:p.Ser28=
NM_005514.8:c.82T= MANE Select NP_005505.2:p.Ser28=