Canonical Allele Identifier: CA368046215

Gene: ABCB1

Linked Data

• dbSNP Id: rs1432511771
• MyVariant Identifiers: chr7:g.87145827G>A (hg19) ; chr7:g.87516511G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87516511G>A , CM000669.2:g.87516511G>A	GRCh38
NC_000007.13:g.87145827G>A , CM000669.1:g.87145827G>A	GRCh37
NC_000007.12:g.86983763G>A	NCBI36
NG_011513.1:g.201738C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000265724.8:c.3082C>T	ENSP00000265724.3:p.Pro1028Ser
ENST00000622132.5:c.3082C>T MANE Select	ENSP00000478255.1:p.Pro1028Ser
ENST00000265724.7:c.3082C>T	ENSP00000265724.3:p.Pro1028Ser
ENST00000475929.5:n.238C>T
ENST00000483831.1:n.640C>T
ENST00000488737.6:n.724C>T
ENST00000496821.5:n.710C>T
ENST00000543898.5:c.2890C>T	ENSP00000444095.1:p.Pro964Ser
ENST00000622132.4:c.3082C>T	ENSP00000478255.1:p.Pro1028Ser
NM_000927.4:c.3082C>T	NP_000918.2:p.Pro1028Ser
NM_001348944.1:c.3082C>T	NP_001335873.1:p.Pro1028Ser
NM_001348945.1:c.3292C>T	NP_001335874.1:p.Pro1098Ser
NM_001348946.1:c.3082C>T	NP_001335875.1:p.Pro1028Ser
NM_001348946.2:c.3082C>T MANE Select	NP_001335875.1:p.Pro1028Ser
NM_000927.5:c.3082C>T	NP_000918.2:p.Pro1028Ser
NM_001348944.2:c.3082C>T	NP_001335873.1:p.Pro1028Ser
NM_001348945.2:c.3292C>T	NP_001335874.1:p.Pro1098Ser