Canonical Allele Identifier: CA2661803014

Gene: ABCB11

Linked Data

• gnomAD v4: 2-168923305-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168923305A>G , CM000664.2:g.168923305A>G	GRCh38
NC_000002.11:g.169779815A>G , CM000664.1:g.169779815A>G	GRCh37
NC_000002.10:g.169488061A>G	NCBI36
NG_007374.1:g.113019T>C
NG_007374.2:g.113092T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648875.1:c.226+1352T>C
ENST00000649448.1:c.2660T>C	ENSP00000497165.1:n.2660T>C
ENST00000650372.1:c.*317T>C MANE Select	ENSP00000497931.1:n.*317T>C
ENST00000263817.6:c.*317T>C	ENSP00000263817.6:n.*317T>C
NM_003742.2:c.*317T>C	NP_003733.2:n.*317T>C
XM_006712817.2:c.*317T>C	XP_006712880.1:n.*317T>C
XM_011512077.1:c.*317T>C	XP_011510379.1:n.*317T>C
XM_011512078.1:c.*271T>C	XP_011510380.1:n.*271T>C
XM_011512079.1:c.*317T>C	XP_011510381.1:n.*317T>C
XM_011512081.1:c.*317T>C	XP_011510383.1:n.*317T>C
NM_003742.4:c.*317T>C MANE Select	NP_003733.2:n.*317T>C
XM_006712817.3:c.*317T>C	XP_006712880.1:n.*317T>C
XM_011512077.2:c.*317T>C	XP_011510379.1:n.*317T>C
XM_011512078.2:c.*271T>C	XP_011510380.1:n.*271T>C
XM_011512081.2:c.*317T>C	XP_011510383.1:n.*317T>C
XM_017005165.1:c.3867+1352T>C	XP_016860654.1:n.3867+1352T>C
XM_017005166.1:c.*317T>C	XP_016860655.1:n.*317T>C
XM_017005167.1:c.*317T>C	XP_016860656.1:n.*317T>C