Canonical Allele Identifier: CA363311425

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355583-T-A
• MyVariant Identifiers: chr6:g.31323360T>A (hg19) ; chr6:g.31355583T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355583T>A , CM000668.2:g.31355583T>A	GRCh38
NC_000006.11:g.31323360T>A , CM000668.1:g.31323360T>A	GRCh37
NC_000006.10:g.31431339T>A	NCBI36
NG_023187.1:g.6630A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2676A>T
ENST00000481849.6:n.2102A>T
ENST00000497377.6:n.2102A>T
ENST00000640094.2:c.629A>T	ENSP00000491275.2:p.Lys210Met
ENST00000696558.1:c.698A>T	ENSP00000512716.1:n.698A>T
ENST00000696559.1:c.629A>T	ENSP00000512717.1:p.Lys210Met
ENST00000696560.1:c.629A>T	ENSP00000512718.1:p.Lys210Met
ENST00000696561.1:c.629A>T	ENSP00000512719.1:p.Lys210Met
ENST00000696562.1:c.629A>T	ENSP00000512720.1:p.Lys210Met
ENST00000412585.7:c.629A>T MANE Select	ENSP00000399168.2:p.Lys210Met
ENST00000412585.6:c.629A>T	ENSP00000399168.2:p.Lys210Met
ENST00000434333.1:c.662A>T	ENSP00000405931.1:p.Lys221Met
ENST00000463574.1:n.220A>T
ENST00000474381.1:n.1078A>T
ENST00000498007.1:n.895A>T
NM_005514.6:c.629A>T	NP_005505.2:p.Lys210Met
XM_011514556.1:c.662A>T	XP_011512858.1:p.Lys221Met
XM_011514557.1:c.629A>T	XP_011512859.1:p.Lys210Met
XR_926175.1:n.1068A>T
NM_005514.7:c.629A>T	NP_005505.2:p.Lys210Met
NM_005514.8:c.629A>T MANE Select	NP_005505.2:p.Lys210Met