Canonical Allele Identifier: CA2581836021

Gene: ABCB11

Genomic Alleles

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

Transcript Alleles

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