Canonical Allele Identifier: CA349124705

Gene: ABCB11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168936342C>A , CM000664.2:g.168936342C>A	GRCh38
NC_000002.11:g.169792852C>A , CM000664.1:g.169792852C>A	GRCh37
NC_000002.10:g.169501098C>A	NCBI36
NG_007374.1:g.99982G>T
NG_007374.2:g.100055G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_003742.4:c.2702G>T MANE Select	NP_003733.2:p.Ser901Ile
ENST00000650372.1:c.2702G>T MANE Select	ENSP00000497931.1:p.Ser901Ile
NM_003742.2:c.2702G>T	NP_003733.2:p.Ser901Ile
ENST00000263817.6:c.2702G>T	ENSP00000263817.6:p.Ser901Ile
ENST00000439188.1:c.1391G>T	ENSP00000416058.1:n.1391G>T
ENST00000649448.1:c.1019G>T	ENSP00000497165.1:p.Ser340Ile
XM_006712817.2:c.2744G>T	XP_006712880.1:p.Ser915Ile
XM_006712817.3:c.2744G>T	XP_006712880.1:p.Ser915Ile
XM_011512077.1:c.2804G>T	XP_011510379.1:p.Ser935Ile
XM_011512077.2:c.2804G>T	XP_011510379.1:p.Ser935Ile
XM_011512078.1:c.2804G>T	XP_011510380.1:p.Ser935Ile
XM_011512078.2:c.2804G>T	XP_011510380.1:p.Ser935Ile
XM_011512079.1:c.2804G>T	XP_011510381.1:p.Ser935Ile
XM_011512080.1:c.2724G>T	XP_011510382.1:p.Glu908Asp
XM_011512080.2:c.2724G>T	XP_011510382.1:p.Glu908Asp
XM_011512081.1:c.1028G>T	XP_011510383.1:p.Ser343Ile
XM_011512081.2:c.1028G>T	XP_011510383.1:p.Ser343Ile
XM_017005165.1:c.2804G>T	XP_016860654.1:p.Ser935Ile
XM_017005166.1:c.2033G>T	XP_016860655.1:p.Ser678Ile
XM_017005167.1:c.1487G>T	XP_016860656.1:p.Ser496Ile