Canonical Allele Identifier: CA449601336
Gene: HLA-B HGNC NCBI

Linked Data

gnomAD v4: 6-31355207-G-T
MyVariant Identifiers: chr6:g.31322984G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355207G>T , CM000668.2:g.31355207G>T GRCh38
NC_000006.11:g.31322984G>T , CM000668.1:g.31322984G>T GRCh37
NC_000006.10:g.31430963G>T NCBI36
NG_023187.1:g.7006C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.2959C>A
ENST00000481849.6:n.2478C>A
ENST00000497377.6:n.2385C>A
ENST00000640094.2:c.895+110C>A ENSP00000491275.2:n.895+110C>A
ENST00000696558.1:c.981C>A ENSP00000512716.1:n.981C>A
ENST00000696559.1:c.912C>A ENSP00000512717.1:p.Ser304=
ENST00000696560.1:c.912C>A ENSP00000512718.1:p.Ser304=
ENST00000696561.1:c.912C>A ENSP00000512719.1:p.Ser304=
ENST00000696562.1:c.912C>A ENSP00000512720.1:p.Ser304=
ENST00000412585.7:c.912C>A MANE Select ENSP00000399168.2:p.Ser304=
ENST00000640094.1:c.88+110C>A ENSP00000491275.1:n.88+110C>A
ENST00000412585.6:c.912C>A ENSP00000399168.2:p.Ser304=
ENST00000463574.1:n.503C>A
NM_005514.6:c.912C>A NP_005505.2:p.Ser304=
XM_011514556.1:c.945C>A XP_011512858.1:p.Ser315=
XM_011514557.1:c.895+110C>A XP_011512859.1:n.895+110C>A
XR_926175.1:n.1351C>A
NM_005514.7:c.912C>A NP_005505.2:p.Ser304=
NM_005514.8:c.912C>A MANE Select NP_005505.2:p.Ser304=