Canonical Allele Identifier: CA15162562
Gene: ABCB11 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169030644G>A , CM000664.2:g.169030644G>A GRCh38
NC_000002.11:g.169887154G>A , CM000664.1:g.169887154G>A GRCh37
NC_000002.10:g.169595400G>A NCBI36
NG_007374.1:g.5680C>T
NG_007374.2:g.5753C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000650372.1:c.-28+581C>T MANE Select ENSP00000497931.1:n.-28+581C>T
ENST00000263817.6:c.-28+581C>T ENSP00000263817.6:n.-28+581C>T
NM_003742.2:c.-28+581C>T NP_003733.2:n.-28+581C>T
XM_006712817.2:c.-28+581C>T XP_006712880.1:n.-28+581C>T
XM_011512077.1:c.-28+581C>T XP_011510379.1:n.-28+581C>T
XM_011512078.1:c.-28+581C>T XP_011510380.1:n.-28+581C>T
XM_011512079.1:c.-28+4217C>T XP_011510381.1:n.-28+4217C>T
XM_011512080.1:c.-28+581C>T XP_011510382.1:n.-28+581C>T
NM_003742.4:c.-28+581C>T MANE Select NP_003733.2:n.-28+581C>T
XM_006712817.3:c.-28+581C>T XP_006712880.1:n.-28+581C>T
XM_011512077.2:c.-28+581C>T XP_011510379.1:n.-28+581C>T
XM_011512078.2:c.-28+581C>T XP_011510380.1:n.-28+581C>T
XM_011512080.2:c.-28+581C>T XP_011510382.1:n.-28+581C>T
XM_017005165.1:c.-28+581C>T XP_016860654.1:n.-28+581C>T
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