Canonical Allele Identifier: CA368045106
Gene: ABCB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87515428T>C , CM000669.2:g.87515428T>C GRCh38
NC_000007.13:g.87144744T>C , CM000669.1:g.87144744T>C GRCh37
NC_000007.12:g.86982680T>C NCBI36
NG_011513.1:g.202821A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.3085A>G ENSP00000265724.3:p.Asn1029Asp
ENST00000622132.5:c.3085A>G MANE Select ENSP00000478255.1:p.Asn1029Asp
ENST00000265724.7:c.3085A>G ENSP00000265724.3:p.Asn1029Asp
ENST00000475929.5:n.241A>G
ENST00000488737.6:n.727A>G
ENST00000496821.5:n.713A>G
ENST00000543898.5:c.2893A>G ENSP00000444095.1:p.Asn965Asp
ENST00000622132.4:c.3085A>G ENSP00000478255.1:p.Asn1029Asp
NM_000927.4:c.3085A>G NP_000918.2:p.Asn1029Asp
NM_001348944.1:c.3085A>G NP_001335873.1:p.Asn1029Asp
NM_001348945.1:c.3295A>G NP_001335874.1:p.Asn1099Asp
NM_001348946.1:c.3085A>G NP_001335875.1:p.Asn1029Asp
NM_001348946.2:c.3085A>G MANE Select NP_001335875.1:p.Asn1029Asp
NM_000927.5:c.3085A>G NP_000918.2:p.Asn1029Asp
NM_001348944.2:c.3085A>G NP_001335873.1:p.Asn1029Asp
NM_001348945.2:c.3295A>G NP_001335874.1:p.Asn1099Asp