Canonical Allele Identifier: CA349126302

Gene: ABCB11

Linked Data

• dbSNP Id: rs1692220170
• MyVariant Identifiers: chr2:g.169801172T>G (hg19) ; chr2:g.168944662T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168944662T>G , CM000664.2:g.168944662T>G	GRCh38
NC_000002.11:g.169801172T>G , CM000664.1:g.169801172T>G	GRCh37
NC_000002.10:g.169509418T>G	NCBI36
NG_007374.1:g.91662A>C
NG_007374.2:g.91735A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649448.1:c.870A>C	ENSP00000497165.1:p.Arg290Ser
ENST00000650372.1:c.2553A>C MANE Select	ENSP00000497931.1:p.Arg851Ser
ENST00000263817.6:c.2553A>C	ENSP00000263817.6:p.Arg851Ser
ENST00000439188.1:c.1242A>C	ENSP00000416058.1:n.1242A>C
NM_003742.2:c.2553A>C	NP_003733.2:p.Arg851Ser
XM_006712817.2:c.2595A>C	XP_006712880.1:p.Arg865Ser
XM_011512077.1:c.2655A>C	XP_011510379.1:p.Arg885Ser
XM_011512078.1:c.2655A>C	XP_011510380.1:p.Arg885Ser
XM_011512079.1:c.2655A>C	XP_011510381.1:p.Arg885Ser
XM_011512080.1:c.2655A>C	XP_011510382.1:p.Arg885Ser
XM_011512081.1:c.879A>C	XP_011510383.1:p.Arg293Ser
NM_003742.4:c.2553A>C MANE Select	NP_003733.2:p.Arg851Ser
XM_006712817.3:c.2595A>C	XP_006712880.1:p.Arg865Ser
XM_011512077.2:c.2655A>C	XP_011510379.1:p.Arg885Ser
XM_011512078.2:c.2655A>C	XP_011510380.1:p.Arg885Ser
XM_011512080.2:c.2655A>C	XP_011510382.1:p.Arg885Ser
XM_011512081.2:c.879A>C	XP_011510383.1:p.Arg293Ser
XM_017005165.1:c.2655A>C	XP_016860654.1:p.Arg885Ser
XM_017005166.1:c.1884A>C	XP_016860655.1:p.Arg628Ser
XM_017005167.1:c.1338A>C	XP_016860656.1:p.Arg446Ser