Canonical Allele Identifier: CA566340056

Gene: HLA-B

Linked Data

• dbSNP Id: rs1461712630
• gnomAD v2: 6-31321812-G-T
• gnomAD v3: 6-31354035-G-T
• gnomAD v4: 6-31354035-G-T
• MyVariant Identifiers: chr6:g.31321812G>T (hg19) ; chr6:g.31354035G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354035G>T , CM000668.2:g.31354035G>T	GRCh38
NC_000006.11:g.31321812G>T , CM000668.1:g.31321812G>T	GRCh37
NC_000006.10:g.31429791G>T	NCBI36
NG_023187.1:g.8178C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3402C>A
ENST00000481849.6:n.3362C>A
ENST00000497377.6:n.3269C>A
ENST00000696558.1:c.1424C>A	ENSP00000512716.1:n.1424C>A
ENST00000696559.1:c.*266C>A	ENSP00000512717.1:n.*266C>A
ENST00000696560.1:c.*266C>A	ENSP00000512718.1:n.*266C>A
ENST00000696561.1:c.*266C>A	ENSP00000512719.1:n.*266C>A
ENST00000696562.1:c.*266C>A	ENSP00000512720.1:n.*266C>A
ENST00000412585.7:c.*266C>A MANE Select	ENSP00000399168.2:n.*266C>A
ENST00000412585.6:c.*266C>A	ENSP00000399168.2:n.*266C>A
ENST00000481849.5:n.590C>A
ENST00000497377.5:n.754C>A
NM_005514.6:c.*266C>A	NP_005505.2:n.*266C>A
XM_011514556.1:c.*266C>A	XP_011512858.1:n.*266C>A
XM_011514557.1:c.*266C>A	XP_011512859.1:n.*266C>A
XR_926175.1:n.1794C>A
NM_005514.7:c.*266C>A	NP_005505.2:n.*266C>A
NM_005514.8:c.*266C>A MANE Select	NP_005505.2:n.*266C>A