Canonical Allele Identifier: CA8042922
Gene: ABCC11 HGNC NCBI

Linked Data

dbSNP Id: rs766159688

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.48167405A>G , CM000678.2:g.48167405A>G GRCh38
NC_000016.9:g.48201316A>G , CM000678.1:g.48201316A>G GRCh37
NC_000016.8:g.46758817A>G NCBI36
NG_011522.1:g.72773T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000356608.7:c.4057-39T>C MANE Select ENSP00000349017.2:n.4057-39T>C
ENST00000353782.9:c.3943-39T>C ENSP00000311326.6:n.3943-39T>C
ENST00000356608.6:c.4057-39T>C ENSP00000349017.2:n.4057-39T>C
ENST00000394747.5:c.4057-39T>C ENSP00000378230.1:n.4057-39T>C
ENST00000394748.5:c.4057-39T>C ENSP00000378231.1:n.4057-39T>C
ENST00000565329.1:n.1357-39T>C
NM_032583.3:c.4057-39T>C NP_115972.2:n.4057-39T>C
NM_033151.3:c.4057-39T>C NP_149163.2:n.4057-39T>C
NM_145186.2:c.3943-39T>C NP_660187.1:n.3943-39T>C
XM_011523396.1:c.3859-39T>C XP_011521698.1:n.3859-39T>C
XM_011523397.1:c.3100-39T>C XP_011521699.1:n.3100-39T>C
XM_011523398.1:c.2188-39T>C XP_011521700.1:n.2188-39T>C
XM_011523397.2:c.3100-39T>C XP_011521699.1:n.3100-39T>C
XM_011523398.3:c.2188-39T>C XP_011521700.1:n.2188-39T>C
XM_017023795.2:c.4057-39T>C XP_016879284.1:n.4057-39T>C
XM_017023796.2:c.4057-39T>C XP_016879285.1:n.4057-39T>C
XM_017023797.2:c.4057-39T>C XP_016879286.1:n.4057-39T>C
XM_017023798.2:c.4057-39T>C XP_016879287.1:n.4057-39T>C
XM_017023799.2:c.4057-39T>C XP_016879288.1:n.4057-39T>C
XM_017023800.2:c.4057-39T>C XP_016879289.1:n.4057-39T>C
XM_017023801.2:c.3949-39T>C XP_016879290.1:n.3949-39T>C
XM_017023802.2:c.3100-39T>C XP_016879291.1:n.3100-39T>C
XM_024450475.1:c.3100-39T>C XP_024306243.1:n.3100-39T>C
XR_001752012.1:n.6735-39T>C
NM_001370496.1:c.4063-39T>C NP_001357425.1:n.4063-39T>C
NM_001370497.1:c.4057-39T>C MANE Select NP_001357426.1:n.4057-39T>C
NM_032583.4:c.4057-39T>C NP_115972.2:n.4057-39T>C
NM_033151.4:c.4057-39T>C NP_149163.2:n.4057-39T>C
NM_145186.3:c.3943-39T>C NP_660187.1:n.3943-39T>C