Canonical Allele Identifier: CA280260643

Gene: ABCC11

Linked Data

• dbSNP Id: rs959840775
• gnomAD v2: 16-48201509-G-A
• gnomAD v3: 16-48167598-G-A
• gnomAD v4: 16-48167598-G-A
• MyVariant Identifiers: chr16:g.48201509G>A (hg19) ; chr16:g.48167598G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.48167598G>A , CM000678.2:g.48167598G>A	GRCh38
NC_000016.9:g.48201509G>A , CM000678.1:g.48201509G>A	GRCh37
NC_000016.8:g.46759010G>A	NCBI36
NG_011522.1:g.72580C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000356608.7:c.3954C>T MANE Select	ENSP00000349017.2:p.Arg1318=
ENST00000353782.9:c.3840C>T	ENSP00000311326.6:p.Arg1280=
ENST00000356608.6:c.3954C>T	ENSP00000349017.2:p.Arg1318=
ENST00000394747.5:c.3954C>T	ENSP00000378230.1:p.Arg1318=
ENST00000394748.5:c.3954C>T	ENSP00000378231.1:p.Arg1318=
ENST00000565329.1:n.1254C>T
NM_032583.3:c.3954C>T	NP_115972.2:p.Arg1318=
NM_033151.3:c.3954C>T	NP_149163.2:p.Arg1318=
NM_145186.2:c.3840C>T	NP_660187.1:p.Arg1280=
XM_011523396.1:c.3756C>T	XP_011521698.1:p.Arg1252=
XM_011523397.1:c.2997C>T	XP_011521699.1:p.Arg999=
XM_011523398.1:c.2085C>T	XP_011521700.1:p.Arg695=
XM_011523397.2:c.2997C>T	XP_011521699.1:p.Arg999=
XM_011523398.3:c.2085C>T	XP_011521700.1:p.Arg695=
XM_017023795.2:c.3954C>T	XP_016879284.1:p.Arg1318=
XM_017023796.2:c.3954C>T	XP_016879285.1:p.Arg1318=
XM_017023797.2:c.3954C>T	XP_016879286.1:p.Arg1318=
XM_017023798.2:c.3954C>T	XP_016879287.1:p.Arg1318=
XM_017023799.2:c.3954C>T	XP_016879288.1:p.Arg1318=
XM_017023800.2:c.3954C>T	XP_016879289.1:p.Arg1318=
XM_017023801.2:c.3846C>T	XP_016879290.1:p.Arg1282=
XM_017023802.2:c.2997C>T	XP_016879291.1:p.Arg999=
XM_024450475.1:c.2997C>T	XP_024306243.1:p.Arg999=
XR_001752012.1:n.6632C>T
NM_001370496.1:c.3960C>T	NP_001357425.1:p.Arg1320=
NM_001370497.1:c.3954C>T MANE Select	NP_001357426.1:p.Arg1318=
NM_032583.4:c.3954C>T	NP_115972.2:p.Arg1318=
NM_033151.4:c.3954C>T	NP_149163.2:p.Arg1318=
NM_145186.3:c.3840C>T	NP_660187.1:p.Arg1280=