Canonical Allele Identifier: CA449791613

Gene: HLA-B

Linked Data

• dbSNP Id: rs1443727365
• gnomAD v2: 6-31324841-T-A
• gnomAD v4: 6-31357064-T-A
• MyVariant Identifiers: chr6:g.31324841T>A (hg19) ; chr6:g.31357064T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357064T>A , CM000668.2:g.31357064T>A	GRCh38
NC_000006.11:g.31324841T>A , CM000668.1:g.31324841T>A	GRCh37
NC_000006.10:g.31432820T>A	NCBI36
NG_023187.1:g.5149A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1546+22A>T
ENST00000481849.6:n.1546+22A>T
ENST00000497377.6:n.1546+22A>T
ENST00000640094.2:c.73+22A>T	ENSP00000491275.2:n.73+22A>T
ENST00000696558.1:c.73+22A>T	ENSP00000512716.1:n.73+22A>T
ENST00000696559.1:c.73+22A>T	ENSP00000512717.1:n.73+22A>T
ENST00000696560.1:c.73+22A>T	ENSP00000512718.1:n.73+22A>T
ENST00000696561.1:c.73+22A>T	ENSP00000512719.1:n.73+22A>T
ENST00000696562.1:c.73+22A>T	ENSP00000512720.1:n.73+22A>T
ENST00000412585.7:c.73+22A>T MANE Select	ENSP00000399168.2:n.73+22A>T
ENST00000412585.6:c.73+22A>T	ENSP00000399168.2:n.73+22A>T
ENST00000434333.1:c.-1A>T	ENSP00000405931.1:n.-1A>T
ENST00000498007.1:n.94+22A>T
ENST00000603274.1:n.418T>A
NM_005514.6:c.73+22A>T	NP_005505.2:n.73+22A>T
XM_011514556.1:c.-1A>T	XP_011512858.1:n.-1A>T
XM_011514557.1:c.73+22A>T	XP_011512859.1:n.73+22A>T
XR_926175.1:n.83+22A>T
NM_005514.7:c.73+22A>T	NP_005505.2:n.73+22A>T
NM_005514.8:c.73+22A>T MANE Select	NP_005505.2:n.73+22A>T