Canonical Allele Identifier: CA363314795

Gene: HLA-B

Linked Data

• dbSNP Id: rs9266197
• gnomAD v3: 6-31357053-G-T
• gnomAD v4: 6-31357053-G-T
• MyVariant Identifiers: chr6:g.31324830G>T (hg19) ; chr6:g.31357053G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357053G>T , CM000668.2:g.31357053G>T	GRCh38
NC_000006.11:g.31324830G>T , CM000668.1:g.31324830G>T	GRCh37
NC_000006.10:g.31432809G>T	NCBI36
NG_023187.1:g.5160C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1546+33C>A
ENST00000481849.6:n.1546+33C>A
ENST00000497377.6:n.1546+33C>A
ENST00000640094.2:c.73+33C>A	ENSP00000491275.2:n.73+33C>A
ENST00000696558.1:c.73+33C>A	ENSP00000512716.1:n.73+33C>A
ENST00000696559.1:c.73+33C>A	ENSP00000512717.1:n.73+33C>A
ENST00000696560.1:c.73+33C>A	ENSP00000512718.1:n.73+33C>A
ENST00000696561.1:c.73+33C>A	ENSP00000512719.1:n.73+33C>A
ENST00000696562.1:c.73+33C>A	ENSP00000512720.1:n.73+33C>A
ENST00000412585.7:c.73+33C>A MANE Select	ENSP00000399168.2:n.73+33C>A
ENST00000412585.6:c.73+33C>A	ENSP00000399168.2:n.73+33C>A
ENST00000434333.1:c.11C>A	ENSP00000405931.1:p.Ala4Asp
ENST00000498007.1:n.94+33C>A
ENST00000603274.1:n.407G>T
NM_005514.6:c.73+33C>A	NP_005505.2:n.73+33C>A
XM_011514556.1:c.11C>A	XP_011512858.1:p.Ala4Asp
XM_011514557.1:c.73+33C>A	XP_011512859.1:n.73+33C>A
XR_926175.1:n.83+33C>A
NM_005514.7:c.73+33C>A	NP_005505.2:n.73+33C>A
NM_005514.8:c.73+33C>A MANE Select	NP_005505.2:n.73+33C>A