Canonical Allele Identifier: CA349126099

Gene: ABCB11

Linked Data

• gnomAD v4: 2-168944625-C-G
• MyVariant Identifiers: chr2:g.169801135C>G (hg19) ; chr2:g.168944625C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168944625C>G , CM000664.2:g.168944625C>G	GRCh38
NC_000002.11:g.169801135C>G , CM000664.1:g.169801135C>G	GRCh37
NC_000002.10:g.169509381C>G	NCBI36
NG_007374.1:g.91699G>C
NG_007374.2:g.91772G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000649448.1:c.907G>C	ENSP00000497165.1:p.Asp303His
ENST00000650372.1:c.2590G>C MANE Select	ENSP00000497931.1:p.Asp864His
ENST00000263817.6:c.2590G>C	ENSP00000263817.6:p.Asp864His
ENST00000439188.1:c.1279G>C	ENSP00000416058.1:n.1279G>C
NM_003742.2:c.2590G>C	NP_003733.2:p.Asp864His
XM_006712817.2:c.2632G>C	XP_006712880.1:p.Asp878His
XM_011512077.1:c.2692G>C	XP_011510379.1:p.Asp898His
XM_011512078.1:c.2692G>C	XP_011510380.1:p.Asp898His
XM_011512079.1:c.2692G>C	XP_011510381.1:p.Asp898His
XM_011512080.1:c.2692G>C	XP_011510382.1:p.Asp898His
XM_011512081.1:c.916G>C	XP_011510383.1:p.Asp306His
NM_003742.4:c.2590G>C MANE Select	NP_003733.2:p.Asp864His
XM_006712817.3:c.2632G>C	XP_006712880.1:p.Asp878His
XM_011512077.2:c.2692G>C	XP_011510379.1:p.Asp898His
XM_011512078.2:c.2692G>C	XP_011510380.1:p.Asp898His
XM_011512080.2:c.2692G>C	XP_011510382.1:p.Asp898His
XM_011512081.2:c.916G>C	XP_011510383.1:p.Asp306His
XM_017005165.1:c.2692G>C	XP_016860654.1:p.Asp898His
XM_017005166.1:c.1921G>C	XP_016860655.1:p.Asp641His
XM_017005167.1:c.1375G>C	XP_016860656.1:p.Asp459His