Canonical Allele Identifier: CA449790869

Gene: HLA-B

Linked Data

• dbSNP Id: rs9266207
• gnomAD v3: 6-31357176-C-A
• gnomAD v4: 6-31357176-C-A
• MyVariant Identifiers: chr6:g.31324953C>A (hg19) ; chr6:g.31357176C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357176C>A , CM000668.2:g.31357176C>A	GRCh38
NC_000006.11:g.31324953C>A , CM000668.1:g.31324953C>A	GRCh37
NC_000006.10:g.31432932C>A	NCBI36
NG_023187.1:g.5037G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1456G>T
ENST00000481849.6:n.1456G>T
ENST00000497377.6:n.1456G>T
ENST00000696559.1:c.-18G>T	ENSP00000512717.1:n.-18G>T
ENST00000696560.1:c.-18G>T	ENSP00000512718.1:n.-18G>T
ENST00000696561.1:c.-18G>T	ENSP00000512719.1:n.-18G>T
ENST00000696562.1:c.-18G>T	ENSP00000512720.1:n.-18G>T
ENST00000412585.7:c.-18G>T MANE Select	ENSP00000399168.2:n.-18G>T
ENST00000412585.6:c.-18G>T	ENSP00000399168.2:n.-18G>T
ENST00000434333.1:c.-113G>T	ENSP00000405931.1:n.-113G>T
ENST00000498007.1:n.4G>T
ENST00000603274.1:n.530C>A
NM_005514.6:c.-18G>T	NP_005505.2:n.-18G>T
NM_005514.7:c.-18G>T	NP_005505.2:n.-18G>T
NM_005514.8:c.-18G>T MANE Select	NP_005505.2:n.-18G>T