Canonical Allele Identifier: CA449790692

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355524-G-A
• MyVariant Identifiers: chr6:g.31323301G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355524G>A , CM000668.2:g.31355524G>A	GRCh38
NC_000006.11:g.31323301G>A , CM000668.1:g.31323301G>A	GRCh37
NC_000006.10:g.31431280G>A	NCBI36
NG_023187.1:g.6689C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2735C>T
ENST00000481849.6:n.2161C>T
ENST00000497377.6:n.2161C>T
ENST00000640094.2:c.688C>T	ENSP00000491275.2:p.Leu230=
ENST00000696558.1:c.757C>T	ENSP00000512716.1:n.757C>T
ENST00000696559.1:c.688C>T	ENSP00000512717.1:p.Leu230=
ENST00000696560.1:c.688C>T	ENSP00000512718.1:p.Leu230=
ENST00000696561.1:c.688C>T	ENSP00000512719.1:p.Leu230=
ENST00000696562.1:c.688C>T	ENSP00000512720.1:p.Leu230=
ENST00000412585.7:c.688C>T MANE Select	ENSP00000399168.2:p.Leu230=
ENST00000412585.6:c.688C>T	ENSP00000399168.2:p.Leu230=
ENST00000434333.1:c.721C>T	ENSP00000405931.1:p.Leu241=
ENST00000463574.1:n.279C>T
ENST00000474381.1:n.1137C>T
ENST00000498007.1:n.954C>T
NM_005514.6:c.688C>T	NP_005505.2:p.Leu230=
XM_011514556.1:c.721C>T	XP_011512858.1:p.Leu241=
XM_011514557.1:c.688C>T	XP_011512859.1:p.Leu230=
XR_926175.1:n.1127C>T
NM_005514.7:c.688C>T	NP_005505.2:p.Leu230=
NM_005514.8:c.688C>T MANE Select	NP_005505.2:p.Leu230=