Canonical Allele Identifier: CA4327895

Gene: ABCB1

Linked Data

• dbSNP Id: rs572038993
• ExAC: 7:87145971 C / G
• gnomAD v2: 7-87145971-C-G
• gnomAD v3: 7-87516655-C-G
• gnomAD v4: 7-87516655-C-G
• MyVariant Identifiers: chr7:g.87145971C>G (hg19) ; chr7:g.87516655C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87516655C>G , CM000669.2:g.87516655C>G	GRCh38
NC_000007.13:g.87145971C>G , CM000669.1:g.87145971C>G	GRCh37
NC_000007.12:g.86983907C>G	NCBI36
NG_011513.1:g.201594G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2938G>C	ENSP00000265724.3:p.Ala980Pro
ENST00000622132.5:c.2938G>C MANE Select	ENSP00000478255.1:p.Ala980Pro
ENST00000265724.7:c.2938G>C	ENSP00000265724.3:p.Ala980Pro
ENST00000475929.5:n.94G>C
ENST00000483831.1:n.496G>C
ENST00000488737.6:n.580G>C
ENST00000496821.5:n.566G>C
ENST00000543898.5:c.2746G>C	ENSP00000444095.1:p.Ala916Pro
ENST00000622132.4:c.2938G>C	ENSP00000478255.1:p.Ala980Pro
NM_000927.4:c.2938G>C	NP_000918.2:p.Ala980Pro
NM_001348944.1:c.2938G>C	NP_001335873.1:p.Ala980Pro
NM_001348945.1:c.3148G>C	NP_001335874.1:p.Ala1050Pro
NM_001348946.1:c.2938G>C	NP_001335875.1:p.Ala980Pro
NM_001348946.2:c.2938G>C MANE Select	NP_001335875.1:p.Ala980Pro
NM_000927.5:c.2938G>C	NP_000918.2:p.Ala980Pro
NM_001348944.2:c.2938G>C	NP_001335873.1:p.Ala980Pro
NM_001348945.2:c.3148G>C	NP_001335874.1:p.Ala1050Pro