Canonical Allele Identifier: CA368046921
Gene: ABCB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87516577C>A , CM000669.2:g.87516577C>A GRCh38
NC_000007.13:g.87145893C>A , CM000669.1:g.87145893C>A GRCh37
NC_000007.12:g.86983829C>A NCBI36
NG_011513.1:g.201672G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.3016G>T ENSP00000265724.3:p.Ala1006Ser
ENST00000622132.5:c.3016G>T MANE Select ENSP00000478255.1:p.Ala1006Ser
ENST00000265724.7:c.3016G>T ENSP00000265724.3:p.Ala1006Ser
ENST00000475929.5:n.172G>T
ENST00000483831.1:n.574G>T
ENST00000488737.6:n.658G>T
ENST00000496821.5:n.644G>T
ENST00000543898.5:c.2824G>T ENSP00000444095.1:p.Ala942Ser
ENST00000622132.4:c.3016G>T ENSP00000478255.1:p.Ala1006Ser
NM_000927.4:c.3016G>T NP_000918.2:p.Ala1006Ser
NM_001348944.1:c.3016G>T NP_001335873.1:p.Ala1006Ser
NM_001348945.1:c.3226G>T NP_001335874.1:p.Ala1076Ser
NM_001348946.1:c.3016G>T NP_001335875.1:p.Ala1006Ser
NM_001348946.2:c.3016G>T MANE Select NP_001335875.1:p.Ala1006Ser
NM_000927.5:c.3016G>T NP_000918.2:p.Ala1006Ser
NM_001348944.2:c.3016G>T NP_001335873.1:p.Ala1006Ser
NM_001348945.2:c.3226G>T NP_001335874.1:p.Ala1076Ser