Canonical Allele Identifier: CA368043468
Gene: ABCB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87515252G>T , CM000669.2:g.87515252G>T GRCh38
NC_000007.13:g.87144568G>T , CM000669.1:g.87144568G>T GRCh37
NC_000007.12:g.86982504G>T NCBI36
NG_011513.1:g.202997C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.3261C>A ENSP00000265724.3:p.Tyr1087Ter
ENST00000622132.5:c.3261C>A MANE Select ENSP00000478255.1:p.Tyr1087Ter
ENST00000265724.7:c.3261C>A ENSP00000265724.3:p.Tyr1087Ter
ENST00000475929.5:n.417C>A
ENST00000488737.6:n.903C>A
ENST00000496821.5:n.889C>A
ENST00000543898.5:c.3069C>A ENSP00000444095.1:p.Tyr1023Ter
ENST00000622132.4:c.3261C>A ENSP00000478255.1:p.Tyr1087Ter
NM_000927.4:c.3261C>A NP_000918.2:p.Tyr1087Ter
NM_001348944.1:c.3261C>A NP_001335873.1:p.Tyr1087Ter
NM_001348945.1:c.3471C>A NP_001335874.1:p.Tyr1157Ter
NM_001348946.1:c.3261C>A NP_001335875.1:p.Tyr1087Ter
NM_001348946.2:c.3261C>A MANE Select NP_001335875.1:p.Tyr1087Ter
NM_000927.5:c.3261C>A NP_000918.2:p.Tyr1087Ter
NM_001348944.2:c.3261C>A NP_001335873.1:p.Tyr1087Ter
NM_001348945.2:c.3471C>A NP_001335874.1:p.Tyr1157Ter