Canonical Allele Identifier: CA1087463937

Gene: HLA-B

Linked Data

• gnomAD v3: 6-31355010-T-TC
• gnomAD v4: 6-31355010-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355010_31355011insC , CM000668.2:g.31355010_31355011insC	GRCh38
NC_000006.11:g.31322787_31322788insC , CM000668.1:g.31322787_31322788insC	GRCh37
NC_000006.10:g.31430766_31430767insC	NCBI36
NG_023187.1:g.7202_7203insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3059+96_3059+97insG
ENST00000481849.6:n.2674_2675insG
ENST00000497377.6:n.2581_2582insG
ENST00000640094.2:c.895+306_895+307insG	ENSP00000491275.2:n.895+306_895+307insG
ENST00000696558.1:c.1081+96_1081+97insG	ENSP00000512716.1:n.1081+96_1081+97insG
ENST00000696559.1:c.1012+96_1012+97insG	ENSP00000512717.1:n.1012+96_1012+97insG
ENST00000696560.1:c.1012+96_1012+97insG	ENSP00000512718.1:n.1012+96_1012+97insG
ENST00000696561.1:c.1012+96_1012+97insG	ENSP00000512719.1:n.1012+96_1012+97insG
ENST00000696562.1:c.1012+96_1012+97insG	ENSP00000512720.1:n.1012+96_1012+97insG
ENST00000412585.7:c.1012+96_1012+97insG MANE Select	ENSP00000399168.2:n.1012+96_1012+97insG
ENST00000640094.1:c.88+306_88+307insG	ENSP00000491275.1:n.88+306_88+307insG
ENST00000412585.6:c.1012+96_1012+97insG	ENSP00000399168.2:n.1012+96_1012+97insG
ENST00000497377.5:n.66_67insG
NM_005514.6:c.1012+96_1012+97insG	NP_005505.2:n.1012+96_1012+97insG
XM_011514556.1:c.1045+96_1045+97insG	XP_011512858.1:n.1045+96_1045+97insG
XM_011514557.1:c.895+306_895+307insG	XP_011512859.1:n.895+306_895+307insG
XR_926175.1:n.1451+96_1451+97insG
NM_005514.7:c.1012+96_1012+97insG	NP_005505.2:n.1012+96_1012+97insG
NM_005514.8:c.1012+96_1012+97insG MANE Select	NP_005505.2:n.1012+96_1012+97insG