Canonical Allele Identifier: CA1619116336
Gene: HLA-B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31353944C= , CM000668.2:g.31353944C= GRCh38
NC_000006.11:g.31321721C= , CM000668.1:g.31321721C= GRCh37
NC_000006.10:g.31429700C= NCBI36
NG_023187.1:g.8269G=

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.3493G=
ENST00000481849.6:n.3453G=
ENST00000497377.6:n.3360G=
ENST00000696558.1:c.1515G= ENSP00000512716.1:n.1515G=
ENST00000696559.1:c.*357G= ENSP00000512717.1:n.*357G=
ENST00000696560.1:c.*357G= ENSP00000512718.1:n.*357G=
ENST00000696561.1:c.*357G= ENSP00000512719.1:n.*357G=
ENST00000696562.1:c.*357G= ENSP00000512720.1:n.*357G=
ENST00000412585.7:c.*357G= MANE Select ENSP00000399168.2:n.*357G=
ENST00000412585.6:c.*357G= ENSP00000399168.2:n.*357G=
ENST00000481849.5:n.681G=
ENST00000497377.5:n.845G=
NM_005514.6:c.*357G= NP_005505.2:n.*357G=
XM_011514556.1:c.*357G= XP_011512858.1:n.*357G=
XM_011514557.1:c.*357G= XP_011512859.1:n.*357G=
XR_926175.1:n.1885G=
NM_005514.7:c.*357G= NP_005505.2:n.*357G=
NM_005514.8:c.*357G= MANE Select NP_005505.2:n.*357G=