Canonical Allele Identifier: CA363308879

Gene: HLA-B

Linked Data

• gnomAD v3: 6-31355167-G-T
• gnomAD v4: 6-31355167-G-T
• MyVariant Identifiers: chr6:g.31322944G>T (hg19) ; chr6:g.31355167G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355167G>T , CM000668.2:g.31355167G>T	GRCh38
NC_000006.11:g.31322944G>T , CM000668.1:g.31322944G>T	GRCh37
NC_000006.10:g.31430923G>T	NCBI36
NG_023187.1:g.7046C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.2999C>A
ENST00000481849.6:n.2518C>A
ENST00000497377.6:n.2425C>A
ENST00000640094.2:c.895+150C>A	ENSP00000491275.2:n.895+150C>A
ENST00000696558.1:c.1021C>A	ENSP00000512716.1:n.1021C>A
ENST00000696559.1:c.952C>A	ENSP00000512717.1:p.Leu318Ile
ENST00000696560.1:c.952C>A	ENSP00000512718.1:p.Leu318Ile
ENST00000696561.1:c.952C>A	ENSP00000512719.1:p.Leu318Ile
ENST00000696562.1:c.952C>A	ENSP00000512720.1:p.Leu318Ile
ENST00000412585.7:c.952C>A MANE Select	ENSP00000399168.2:p.Leu318Ile
ENST00000640094.1:c.88+150C>A	ENSP00000491275.1:n.88+150C>A
ENST00000412585.6:c.952C>A	ENSP00000399168.2:p.Leu318Ile
ENST00000463574.1:n.543C>A
NM_005514.6:c.952C>A	NP_005505.2:p.Leu318Ile
XM_011514556.1:c.985C>A	XP_011512858.1:p.Leu329Ile
XM_011514557.1:c.895+150C>A	XP_011512859.1:n.895+150C>A
XR_926175.1:n.1391C>A
NM_005514.7:c.952C>A	NP_005505.2:p.Leu318Ile
NM_005514.8:c.952C>A MANE Select	NP_005505.2:p.Leu318Ile