Canonical Allele Identifier: CA2210065054
Gene: ABCC1 HGNC NCBI

Linked Data

dbSNP Id: rs2048331784

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16025225A>G , CM000678.2:g.16025225A>G GRCh38
NC_000016.9:g.16119082A>G , CM000678.1:g.16119082A>G GRCh37
NC_000016.8:g.16026583A>G NCBI36
NG_028268.1:g.80649A>G
NG_028268.2:g.80649A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000399408.7:c.616-7884A>G ENSP00000382340.4:n.616-7884A>G
ENST00000399410.8:c.616-7884A>G MANE Select ENSP00000382342.3:n.616-7884A>G
ENST00000572882.3:c.616-7884A>G ENSP00000461615.2:n.616-7884A>G
ENST00000574224.2:n.691-7884A>G
ENST00000677164.1:c.490-7884A>G ENSP00000502873.1:n.490-7884A>G
ENST00000678422.1:c.616-7884A>G ENSP00000503954.1:n.616-7884A>G
ENST00000679043.1:n.568-7884A>G
ENST00000399408.6:c.-363-7884A>G ENSP00000382340.3:n.-363-7884A>G
ENST00000399410.7:c.616-7884A>G ENSP00000382342.3:n.616-7884A>G
ENST00000572882.2:c.311-7884A>G
ENST00000574224.1:n.216-7884A>G
NM_004996.3:c.616-7884A>G NP_004987.2:n.616-7884A>G
XM_011522497.1:c.592-7884A>G XP_011520799.1:n.592-7884A>G
XM_011522498.1:c.670-7884A>G XP_011520800.1:n.670-7884A>G
XM_011522498.2:c.670-7884A>G XP_011520800.1:n.670-7884A>G
XM_017023237.1:c.670-7884A>G XP_016878726.1:n.670-7884A>G
XM_017023238.1:c.544-7884A>G XP_016878727.1:n.544-7884A>G
XM_017023239.1:c.532-7884A>G XP_016878728.1:n.532-7884A>G
XM_017023240.1:c.670-7884A>G XP_016878729.1:n.670-7884A>G
XM_017023241.1:c.406-7884A>G XP_016878730.1:n.406-7884A>G
XM_017023242.1:c.670-7884A>G XP_016878731.1:n.670-7884A>G
XM_017023243.2:c.670-7884A>G XP_016878732.1:n.670-7884A>G
NM_004996.4:c.616-7884A>G MANE Select NP_004987.2:n.616-7884A>G