Canonical Allele Identifier: CA2661808330

Gene: ABCB11

Linked Data

• gnomAD v4: 2-168996622-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168996622A>G , CM000664.2:g.168996622A>G	GRCh38
NC_000002.11:g.169853132A>G , CM000664.1:g.169853132A>G	GRCh37
NC_000002.10:g.169561378A>G	NCBI36
NG_007374.1:g.39702T>C
NG_007374.2:g.39775T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000650372.1:c.477+13T>C MANE Select	ENSP00000497931.1:n.477+13T>C
ENST00000263817.6:c.477+13T>C	ENSP00000263817.6:n.477+13T>C
NM_003742.2:c.477+13T>C	NP_003733.2:n.477+13T>C
XM_006712817.2:c.519+13T>C	XP_006712880.1:n.519+13T>C
XM_011512077.1:c.579+13T>C	XP_011510379.1:n.579+13T>C
XM_011512078.1:c.579+13T>C	XP_011510380.1:n.579+13T>C
XM_011512079.1:c.579+13T>C	XP_011510381.1:n.579+13T>C
XM_011512080.1:c.579+13T>C	XP_011510382.1:n.579+13T>C
NM_003742.4:c.477+13T>C MANE Select	NP_003733.2:n.477+13T>C
XM_006712817.3:c.519+13T>C	XP_006712880.1:n.519+13T>C
XM_011512077.2:c.579+13T>C	XP_011510379.1:n.579+13T>C
XM_011512078.2:c.579+13T>C	XP_011510380.1:n.579+13T>C
XM_011512080.2:c.579+13T>C	XP_011510382.1:n.579+13T>C
XM_017005165.1:c.579+13T>C	XP_016860654.1:n.579+13T>C