Canonical Allele Identifier: CA2677955539

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355761-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355761G>A , CM000668.2:g.31355761G>A	GRCh38
NC_000006.11:g.31323538G>A , CM000668.1:g.31323538G>A	GRCh37
NC_000006.10:g.31431517G>A	NCBI36
NG_023187.1:g.6452C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.2498C>T
ENST00000481849.6:n.2093-169C>T
ENST00000497377.6:n.2093-169C>T
ENST00000640094.2:c.620-169C>T	ENSP00000491275.2:n.620-169C>T
ENST00000696558.1:c.665C>T	ENSP00000512716.1:p.Ser222Phe
ENST00000696559.1:c.620-169C>T	ENSP00000512717.1:n.620-169C>T
ENST00000696560.1:c.620-169C>T	ENSP00000512718.1:n.620-169C>T
ENST00000696561.1:c.620-169C>T	ENSP00000512719.1:n.620-169C>T
ENST00000696562.1:c.620-169C>T	ENSP00000512720.1:n.620-169C>T
ENST00000412585.7:c.620-169C>T MANE Select	ENSP00000399168.2:n.620-169C>T
ENST00000412585.6:c.620-169C>T	ENSP00000399168.2:n.620-169C>T
ENST00000434333.1:c.653-169C>T	ENSP00000405931.1:n.653-169C>T
ENST00000463574.1:n.42C>T
ENST00000474381.1:n.900C>T
ENST00000498007.1:n.886-169C>T
NM_005514.6:c.620-169C>T	NP_005505.2:n.620-169C>T
XM_011514556.1:c.653-169C>T	XP_011512858.1:n.653-169C>T
XM_011514557.1:c.620-169C>T	XP_011512859.1:n.620-169C>T
XR_926175.1:n.1035C>T
NM_005514.7:c.620-169C>T	NP_005505.2:n.620-169C>T
NM_005514.8:c.620-169C>T MANE Select	NP_005505.2:n.620-169C>T