Canonical Allele Identifier: CA136834171

Gene: HLA-B

Linked Data

• dbSNP Id: rs72558117
• gnomAD v3: 6-31356281-G-T
• gnomAD v4: 6-31356281-G-T
• MyVariant Identifiers: chr6:g.31324058G>T (hg19) ; chr6:g.31356281G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356281G>T , CM000668.2:g.31356281G>T	GRCh38
NC_000006.11:g.31324058G>T , CM000668.1:g.31324058G>T	GRCh37
NC_000006.10:g.31432037G>T	NCBI36
NG_023187.1:g.5932C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1978C>A
ENST00000481849.6:n.1978C>A
ENST00000497377.6:n.1978C>A
ENST00000640094.2:c.505C>A	ENSP00000491275.2:p.Arg169Ser
ENST00000696558.1:c.505C>A	ENSP00000512716.1:p.Arg169Ser
ENST00000696559.1:c.505C>A	ENSP00000512717.1:p.Arg169Ser
ENST00000696560.1:c.505C>A	ENSP00000512718.1:p.Arg169Ser
ENST00000696561.1:c.505C>A	ENSP00000512719.1:p.Arg169Ser
ENST00000696562.1:c.505C>A	ENSP00000512720.1:p.Arg169Ser
ENST00000412585.7:c.505C>A MANE Select	ENSP00000399168.2:p.Arg169Ser
ENST00000412585.6:c.505C>A	ENSP00000399168.2:p.Arg169Ser
ENST00000434333.1:c.538C>A	ENSP00000405931.1:p.Arg180Ser
ENST00000474381.1:n.380C>A
ENST00000498007.1:n.771C>A
NM_005514.6:c.505C>A	NP_005505.2:p.Arg169Ser
XM_011514556.1:c.538C>A	XP_011512858.1:p.Arg180Ser
XM_011514557.1:c.505C>A	XP_011512859.1:p.Arg169Ser
XR_926175.1:n.515C>A
NM_005514.7:c.505C>A	NP_005505.2:p.Arg169Ser
NM_005514.8:c.505C>A MANE Select	NP_005505.2:p.Arg169Ser