Canonical Allele Identifier: CA349127413

Gene: ABCB11

Linked Data

• gnomAD v4: 2-168944879-G-T
• MyVariant Identifiers: chr2:g.169801389G>T (hg19) ; chr2:g.168944879G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168944879G>T , CM000664.2:g.168944879G>T	GRCh38
NC_000002.11:g.169801389G>T , CM000664.1:g.169801389G>T	GRCh37
NC_000002.10:g.169509635G>T	NCBI36
NG_007374.1:g.91445C>A
NG_007374.2:g.91518C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649448.1:c.743C>A	ENSP00000497165.1:p.Ser248Tyr
ENST00000650372.1:c.2426C>A MANE Select	ENSP00000497931.1:p.Ser809Tyr
ENST00000263817.6:c.2426C>A	ENSP00000263817.6:p.Ser809Tyr
ENST00000439188.1:c.1115C>A	ENSP00000416058.1:n.1115C>A
NM_003742.2:c.2426C>A	NP_003733.2:p.Ser809Tyr
XM_006712817.2:c.2468C>A	XP_006712880.1:p.Ser823Tyr
XM_011512077.1:c.2528C>A	XP_011510379.1:p.Ser843Tyr
XM_011512078.1:c.2528C>A	XP_011510380.1:p.Ser843Tyr
XM_011512079.1:c.2528C>A	XP_011510381.1:p.Ser843Tyr
XM_011512080.1:c.2528C>A	XP_011510382.1:p.Ser843Tyr
XM_011512081.1:c.752C>A	XP_011510383.1:p.Ser251Tyr
NM_003742.4:c.2426C>A MANE Select	NP_003733.2:p.Ser809Tyr
XM_006712817.3:c.2468C>A	XP_006712880.1:p.Ser823Tyr
XM_011512077.2:c.2528C>A	XP_011510379.1:p.Ser843Tyr
XM_011512078.2:c.2528C>A	XP_011510380.1:p.Ser843Tyr
XM_011512080.2:c.2528C>A	XP_011510382.1:p.Ser843Tyr
XM_011512081.2:c.752C>A	XP_011510383.1:p.Ser251Tyr
XM_017005165.1:c.2528C>A	XP_016860654.1:p.Ser843Tyr
XM_017005166.1:c.1757C>A	XP_016860655.1:p.Ser586Tyr
XM_017005167.1:c.1211C>A	XP_016860656.1:p.Ser404Tyr