Canonical Allele Identifier: CA2770503562

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355038_31355039insG , CM000668.2:g.31355038_31355039insG	GRCh38
NC_000006.11:g.31322815_31322816insG , CM000668.1:g.31322815_31322816insG	GRCh37
NC_000006.10:g.31430794_31430795insG	NCBI36
NG_023187.1:g.7174_7175insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3059+68_3059+69insC
ENST00000481849.6:n.2646_2647insC
ENST00000497377.6:n.2553_2554insC
ENST00000640094.2:c.895+278_895+279insC	ENSP00000491275.2:n.895+278_895+279insC
ENST00000696558.1:c.1081+68_1081+69insC	ENSP00000512716.1:n.1081+68_1081+69insC
ENST00000696559.1:c.1012+68_1012+69insC	ENSP00000512717.1:n.1012+68_1012+69insC
ENST00000696560.1:c.1012+68_1012+69insC	ENSP00000512718.1:n.1012+68_1012+69insC
ENST00000696561.1:c.1012+68_1012+69insC	ENSP00000512719.1:n.1012+68_1012+69insC
ENST00000696562.1:c.1012+68_1012+69insC	ENSP00000512720.1:n.1012+68_1012+69insC
ENST00000412585.7:c.1012+68_1012+69insC MANE Select	ENSP00000399168.2:n.1012+68_1012+69insC
ENST00000640094.1:c.88+278_88+279insC	ENSP00000491275.1:n.88+278_88+279insC
ENST00000412585.6:c.1012+68_1012+69insC	ENSP00000399168.2:n.1012+68_1012+69insC
ENST00000497377.5:n.38_39insC
NM_005514.6:c.1012+68_1012+69insC	NP_005505.2:n.1012+68_1012+69insC
XM_011514556.1:c.1045+68_1045+69insC	XP_011512858.1:n.1045+68_1045+69insC
XM_011514557.1:c.895+278_895+279insC	XP_011512859.1:n.895+278_895+279insC
XR_926175.1:n.1451+68_1451+69insC
NM_005514.7:c.1012+68_1012+69insC	NP_005505.2:n.1012+68_1012+69insC
NM_005514.8:c.1012+68_1012+69insC MANE Select	NP_005505.2:n.1012+68_1012+69insC