Canonical Allele Identifier: CA136836554
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs151341161
gnomAD v4: 6-31356790-G-A
MyVariant Identifiers: chr6:g.31324567G>A (hg19) chr6:g.31356790G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356790G>A , CM000668.2:g.31356790G>A GRCh38
NC_000006.11:g.31324567G>A , CM000668.1:g.31324567G>A GRCh37
NC_000006.10:g.31432546G>A NCBI36
NG_023187.1:g.5423C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.1714C>T
ENST00000481849.6:n.1714C>T
ENST00000497377.6:n.1714C>T
ENST00000640094.2:c.241C>T ENSP00000491275.2:p.Pro81Ser
ENST00000696558.1:c.241C>T ENSP00000512716.1:p.Pro81Ser
ENST00000696559.1:c.241C>T ENSP00000512717.1:p.Pro81Ser
ENST00000696560.1:c.241C>T ENSP00000512718.1:p.Pro81Ser
ENST00000696561.1:c.241C>T ENSP00000512719.1:p.Pro81Ser
ENST00000696562.1:c.241C>T ENSP00000512720.1:p.Pro81Ser
ENST00000412585.7:c.241C>T MANE Select ENSP00000399168.2:p.Pro81Ser
ENST00000412585.6:c.241C>T ENSP00000399168.2:p.Pro81Ser
ENST00000434333.1:c.274C>T ENSP00000405931.1:p.Pro92Ser
ENST00000474381.1:n.116C>T
ENST00000498007.1:n.262C>T
ENST00000603274.1:n.144G>A
NM_005514.6:c.241C>T NP_005505.2:p.Pro81Ser
XM_011514556.1:c.274C>T XP_011512858.1:p.Pro92Ser
XM_011514557.1:c.241C>T XP_011512859.1:p.Pro81Ser
XR_926175.1:n.251C>T
NM_005514.7:c.241C>T NP_005505.2:p.Pro81Ser
NM_005514.8:c.241C>T MANE Select NP_005505.2:p.Pro81Ser
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