Canonical Allele Identifier: CA2661802306

Gene: ABCB11

Linked Data

• gnomAD v4: 2-168922879-TAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168922882_168922883del , CM000664.2:g.168922882_168922883del	GRCh38
NC_000002.11:g.169779392_169779393del , CM000664.1:g.169779392_169779393del	GRCh37
NC_000002.10:g.169487638_169487639del	NCBI36
NG_007374.1:g.113443_113444del
NG_007374.2:g.113516_113517del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648875.1:c.226+1776_226+1777del
ENST00000650372.1:c.*741_*742del MANE Select	ENSP00000497931.1:n.*741_*742del
XM_006712817.2:c.*741_*742del	XP_006712880.1:n.*741_*742del
XM_011512077.1:c.*741_*742del	XP_011510379.1:n.*741_*742del
XM_011512078.1:c.*695_*696del	XP_011510380.1:n.*695_*696del
XM_011512079.1:c.*741_*742del	XP_011510381.1:n.*741_*742del
XM_011512081.1:c.*741_*742del	XP_011510383.1:n.*741_*742del
NM_003742.4:c.*741_*742del MANE Select	NP_003733.2:n.*741_*742del
XM_006712817.3:c.*741_*742del	XP_006712880.1:n.*741_*742del
XM_011512077.2:c.*741_*742del	XP_011510379.1:n.*741_*742del
XM_011512078.2:c.*695_*696del	XP_011510380.1:n.*695_*696del
XM_011512081.2:c.*741_*742del	XP_011510383.1:n.*741_*742del
XM_017005165.1:c.3867+1776_3867+1777del	XP_016860654.1:n.3867+1776_3867+1777del
XM_017005166.1:c.*741_*742del	XP_016860655.1:n.*741_*742del
XM_017005167.1:c.*741_*742del	XP_016860656.1:n.*741_*742del