Canonical Allele Identifier: CA2661807732

Gene: ABCB11

Linked Data

• gnomAD v4: 2-168990737-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168990737A>G , CM000664.2:g.168990737A>G	GRCh38
NC_000002.11:g.169847247A>G , CM000664.1:g.169847247A>G	GRCh37
NC_000002.10:g.169555493A>G	NCBI36
NG_007374.1:g.45587T>C
NG_007374.2:g.45660T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000650372.1:c.908+64T>C MANE Select	ENSP00000497931.1:n.908+64T>C
ENST00000263817.6:c.908+64T>C	ENSP00000263817.6:n.908+64T>C
NM_003742.2:c.908+64T>C	NP_003733.2:n.908+64T>C
XM_006712817.2:c.950+64T>C	XP_006712880.1:n.950+64T>C
XM_011512077.1:c.1010+64T>C	XP_011510379.1:n.1010+64T>C
XM_011512078.1:c.1010+64T>C	XP_011510380.1:n.1010+64T>C
XM_011512079.1:c.1010+64T>C	XP_011510381.1:n.1010+64T>C
XM_011512080.1:c.1010+64T>C	XP_011510382.1:n.1010+64T>C
NM_003742.4:c.908+64T>C MANE Select	NP_003733.2:n.908+64T>C
XM_006712817.3:c.950+64T>C	XP_006712880.1:n.950+64T>C
XM_011512077.2:c.1010+64T>C	XP_011510379.1:n.1010+64T>C
XM_011512078.2:c.1010+64T>C	XP_011510380.1:n.1010+64T>C
XM_011512080.2:c.1010+64T>C	XP_011510382.1:n.1010+64T>C
XM_017005165.1:c.1010+64T>C	XP_016860654.1:n.1010+64T>C
XM_017005166.1:c.239+64T>C	XP_016860655.1:n.239+64T>C