Canonical Allele Identifier: CA136833700
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs151341321
gnomAD v4: 6-31356212-G-A
MyVariant Identifiers: chr6:g.31323989G>A (hg19) chr6:g.31356212G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356212G>A , CM000668.2:g.31356212G>A GRCh38
NC_000006.11:g.31323989G>A , CM000668.1:g.31323989G>A GRCh37
NC_000006.10:g.31431968G>A NCBI36
NG_023187.1:g.6001C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.2047C>T
ENST00000481849.6:n.2047C>T
ENST00000497377.6:n.2047C>T
ENST00000640094.2:c.574C>T ENSP00000491275.2:p.Leu192Phe
ENST00000696558.1:c.574C>T ENSP00000512716.1:p.Leu192Phe
ENST00000696559.1:c.574C>T ENSP00000512717.1:p.Leu192Phe
ENST00000696560.1:c.574C>T ENSP00000512718.1:p.Leu192Phe
ENST00000696561.1:c.574C>T ENSP00000512719.1:p.Leu192Phe
ENST00000696562.1:c.574C>T ENSP00000512720.1:p.Leu192Phe
ENST00000412585.7:c.574C>T MANE Select ENSP00000399168.2:p.Leu192Phe
ENST00000412585.6:c.574C>T ENSP00000399168.2:p.Leu192Phe
ENST00000434333.1:c.607C>T ENSP00000405931.1:p.Leu203Phe
ENST00000474381.1:n.449C>T
ENST00000498007.1:n.840C>T
NM_005514.6:c.574C>T NP_005505.2:p.Leu192Phe
XM_011514556.1:c.607C>T XP_011512858.1:p.Leu203Phe
XM_011514557.1:c.574C>T XP_011512859.1:p.Leu192Phe
XR_926175.1:n.584C>T
NM_005514.7:c.574C>T NP_005505.2:p.Leu192Phe
NM_005514.8:c.574C>T MANE Select NP_005505.2:p.Leu192Phe
Search 100 bp 5'
Search 100 bp 3'