Canonical Allele Identifier: CA3711176

Gene: HLA-B

Linked Data

• dbSNP Id: rs746224942
• ExAC: 6:31322264 G / T
• gnomAD v2: 6-31322264-G-T
• gnomAD v3: 6-31354487-G-T
• gnomAD v4: 6-31354487-G-T
• MyVariant Identifiers: chr6:g.31322264G>T (hg19) ; chr6:g.31354487G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354487G>T , CM000668.2:g.31354487G>T	GRCh38
NC_000006.11:g.31322264G>T , CM000668.1:g.31322264G>T	GRCh37
NC_000006.10:g.31430243G>T	NCBI36
NG_023187.1:g.7726C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3132C>A
ENST00000481849.6:n.3092C>A
ENST00000497377.6:n.2999C>A
ENST00000640094.2:c.968C>A	ENSP00000491275.2:p.Ala323Asp
ENST00000696558.1:c.1154C>A	ENSP00000512716.1:n.1154C>A
ENST00000696559.1:c.1085C>A	ENSP00000512717.1:p.Ala362Asp
ENST00000696560.1:c.1085C>A	ENSP00000512718.1:p.Ala362Asp
ENST00000696561.1:c.1085C>A	ENSP00000512719.1:p.Ala362Asp
ENST00000696562.1:c.1085C>A	ENSP00000512720.1:p.Ala362Asp
ENST00000412585.7:c.1085C>A MANE Select	ENSP00000399168.2:p.Ala362Asp
ENST00000412585.6:c.1085C>A	ENSP00000399168.2:p.Ala362Asp
ENST00000481849.5:n.320C>A
ENST00000497377.5:n.484C>A
NM_005514.6:c.1085C>A	NP_005505.2:p.Ala362Asp
XM_011514556.1:c.1118C>A	XP_011512858.1:p.Ala373Asp
XM_011514557.1:c.968C>A	XP_011512859.1:p.Ala323Asp
XR_926175.1:n.1524C>A
NM_005514.7:c.1085C>A	NP_005505.2:p.Ala362Asp
NM_005514.8:c.1085C>A MANE Select	NP_005505.2:p.Ala362Asp