Canonical Allele Identifier: CA449790830

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31357161-C-A
• MyVariant Identifiers: chr6:g.31324938C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357161C>A , CM000668.2:g.31357161C>A	GRCh38
NC_000006.11:g.31324938C>A , CM000668.1:g.31324938C>A	GRCh37
NC_000006.10:g.31432917C>A	NCBI36
NG_023187.1:g.5052G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1471G>T
ENST00000481849.6:n.1471G>T
ENST00000497377.6:n.1471G>T
ENST00000696559.1:c.-3G>T	ENSP00000512717.1:n.-3G>T
ENST00000696560.1:c.-3G>T	ENSP00000512718.1:n.-3G>T
ENST00000696561.1:c.-3G>T	ENSP00000512719.1:n.-3G>T
ENST00000696562.1:c.-3G>T	ENSP00000512720.1:n.-3G>T
ENST00000412585.7:c.-3G>T MANE Select	ENSP00000399168.2:n.-3G>T
ENST00000412585.6:c.-3G>T	ENSP00000399168.2:n.-3G>T
ENST00000434333.1:c.-98G>T	ENSP00000405931.1:n.-98G>T
ENST00000498007.1:n.19G>T
ENST00000603274.1:n.515C>A
NM_005514.6:c.-3G>T	NP_005505.2:n.-3G>T
XM_011514557.1:c.-3G>T	XP_011512859.1:n.-3G>T
XR_926175.1:n.8G>T
NM_005514.7:c.-3G>T	NP_005505.2:n.-3G>T
NM_005514.8:c.-3G>T MANE Select	NP_005505.2:n.-3G>T