Canonical Allele Identifier: CA2210093137
Gene: ABCC1 HGNC NCBI

Linked Data

dbSNP Id: rs35621

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16074751C>G , CM000678.2:g.16074751C>G GRCh38
NC_000016.9:g.16168608C>G , CM000678.1:g.16168608C>G GRCh37
NC_000016.8:g.16076109C>G NCBI36
NG_028268.1:g.130175C>G
NG_028268.2:g.130175C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000399408.7:c.1913-1575C>G ENSP00000382340.4:n.1913-1575C>G
ENST00000399410.8:c.1913-1575C>G MANE Select ENSP00000382342.3:n.1913-1575C>G
ENST00000572882.3:c.1913-1575C>G ENSP00000461615.2:n.1913-1575C>G
ENST00000677164.1:c.1787-1575C>G ENSP00000502873.1:n.1787-1575C>G
ENST00000678422.1:c.1913-1575C>G ENSP00000503954.1:n.1913-1575C>G
ENST00000399408.6:c.935-1575C>G ENSP00000382340.3:n.935-1575C>G
ENST00000399410.7:c.1913-1575C>G ENSP00000382342.3:n.1913-1575C>G
ENST00000572882.2:c.1608-1575C>G
NM_004996.3:c.1913-1575C>G NP_004987.2:n.1913-1575C>G
XM_011522497.1:c.1889-1575C>G XP_011520799.1:n.1889-1575C>G
XM_011522498.1:c.1820-1575C>G XP_011520800.1:n.1820-1575C>G
XM_011522498.2:c.1820-1575C>G XP_011520800.1:n.1820-1575C>G
XM_017023237.1:c.1967-1575C>G XP_016878726.1:n.1967-1575C>G
XM_017023238.1:c.1841-1575C>G XP_016878727.1:n.1841-1575C>G
XM_017023239.1:c.1829-1575C>G XP_016878728.1:n.1829-1575C>G
XM_017023240.1:c.1967-1575C>G XP_016878729.1:n.1967-1575C>G
XM_017023241.1:c.1703-1575C>G XP_016878730.1:n.1703-1575C>G
XM_017023242.1:c.1967-1575C>G XP_016878731.1:n.1967-1575C>G
XM_017023243.2:c.1967-1575C>G XP_016878732.1:n.1967-1575C>G
NM_004996.4:c.1913-1575C>G MANE Select NP_004987.2:n.1913-1575C>G