Canonical Allele Identifier: CA2581836022

Gene: ABCB11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.169030644G>T , CM000664.2:g.169030644G>T	GRCh38
NC_000002.11:g.169887154G>T , CM000664.1:g.169887154G>T	GRCh37
NC_000002.10:g.169595400G>T	NCBI36
NG_007374.1:g.5680C>A
NG_007374.2:g.5753C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650372.1:c.-28+581C>A MANE Select	ENSP00000497931.1:n.-28+581C>A
ENST00000263817.6:c.-28+581C>A	ENSP00000263817.6:n.-28+581C>A
NM_003742.2:c.-28+581C>A	NP_003733.2:n.-28+581C>A
XM_006712817.2:c.-28+581C>A	XP_006712880.1:n.-28+581C>A
XM_011512077.1:c.-28+581C>A	XP_011510379.1:n.-28+581C>A
XM_011512078.1:c.-28+581C>A	XP_011510380.1:n.-28+581C>A
XM_011512079.1:c.-28+4217C>A	XP_011510381.1:n.-28+4217C>A
XM_011512080.1:c.-28+581C>A	XP_011510382.1:n.-28+581C>A
NM_003742.4:c.-28+581C>A MANE Select	NP_003733.2:n.-28+581C>A
XM_006712817.3:c.-28+581C>A	XP_006712880.1:n.-28+581C>A
XM_011512077.2:c.-28+581C>A	XP_011510379.1:n.-28+581C>A
XM_011512078.2:c.-28+581C>A	XP_011510380.1:n.-28+581C>A
XM_011512080.2:c.-28+581C>A	XP_011510382.1:n.-28+581C>A
XM_017005165.1:c.-28+581C>A	XP_016860654.1:n.-28+581C>A