Canonical Allele Identifier: CA3711382
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs148982608
gnomAD v3: 6-31355561-G-A
gnomAD v4: 6-31355561-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355561G>A , CM000668.2:g.31355561G>A GRCh38
NC_000006.11:g.31323338G>A , CM000668.1:g.31323338G>A GRCh37
NC_000006.10:g.31431317G>A NCBI36
NG_023187.1:g.6652C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.2698C>T
ENST00000481849.6:n.2124C>T
ENST00000497377.6:n.2124C>T
ENST00000640094.2:c.651C>T ENSP00000491275.2:p.Pro217=
ENST00000696558.1:c.720C>T ENSP00000512716.1:n.720C>T
ENST00000696559.1:c.651C>T ENSP00000512717.1:p.Pro217=
ENST00000696560.1:c.651C>T ENSP00000512718.1:p.Pro217=
ENST00000696561.1:c.651C>T ENSP00000512719.1:p.Pro217=
ENST00000696562.1:c.651C>T ENSP00000512720.1:p.Pro217=
ENST00000412585.7:c.651C>T MANE Select ENSP00000399168.2:p.Pro217=
ENST00000412585.6:c.651C>T ENSP00000399168.2:p.Pro217=
ENST00000434333.1:c.684C>T ENSP00000405931.1:p.Pro228=
ENST00000463574.1:n.242C>T
ENST00000474381.1:n.1100C>T
ENST00000498007.1:n.917C>T
NM_005514.6:c.651C>T NP_005505.2:p.Pro217=
XM_011514556.1:c.684C>T XP_011512858.1:p.Pro228=
XM_011514557.1:c.651C>T XP_011512859.1:p.Pro217=
XR_926175.1:n.1090C>T
NM_005514.7:c.651C>T NP_005505.2:p.Pro217=
NM_005514.8:c.651C>T MANE Select NP_005505.2:p.Pro217=