Canonical Allele Identifier: CA2683605214

Gene: ABCB1

Linked Data

• gnomAD v4: 7-87515527-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87515527T>C , CM000669.2:g.87515527T>C	GRCh38
NC_000007.13:g.87144843T>C , CM000669.1:g.87144843T>C	GRCh37
NC_000007.12:g.86982779T>C	NCBI36
NG_011513.1:g.202722A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.3085-99A>G	ENSP00000265724.3:n.3085-99A>G
ENST00000622132.5:c.3085-99A>G MANE Select	ENSP00000478255.1:n.3085-99A>G
ENST00000265724.7:c.3085-99A>G	ENSP00000265724.3:n.3085-99A>G
ENST00000475929.5:n.241-99A>G
ENST00000488737.6:n.727-99A>G
ENST00000496821.5:n.713-99A>G
ENST00000543898.5:c.2893-99A>G	ENSP00000444095.1:n.2893-99A>G
ENST00000622132.4:c.3085-99A>G	ENSP00000478255.1:n.3085-99A>G
NM_000927.4:c.3085-99A>G	NP_000918.2:n.3085-99A>G
NM_001348944.1:c.3085-99A>G	NP_001335873.1:n.3085-99A>G
NM_001348945.1:c.3295-99A>G	NP_001335874.1:n.3295-99A>G
NM_001348946.1:c.3085-99A>G	NP_001335875.1:n.3085-99A>G
NM_001348946.2:c.3085-99A>G MANE Select	NP_001335875.1:n.3085-99A>G
NM_000927.5:c.3085-99A>G	NP_000918.2:n.3085-99A>G
NM_001348944.2:c.3085-99A>G	NP_001335873.1:n.3085-99A>G
NM_001348945.2:c.3295-99A>G	NP_001335874.1:n.3295-99A>G