Canonical Allele Identifier: CA1931484673
Gene: ABCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99851546C= , CM000672.2:g.99851546C= GRCh38
NC_000010.10:g.101611303C= , CM000672.1:g.101611303C= GRCh37
NC_000010.9:g.101601293C= NCBI36
NG_011798.1:g.73841C=
NG_011798.2:g.73949C=

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.4553C= MANE Select ENSP00000497274.1:p.Pro1518=
ENST00000648523.1:c.623C=
ENST00000370449.8:c.4553C= ENSP00000359478.4:p.Pro1518=
NM_000392.4:c.4553C= NP_000383.1:p.Pro1518=
XM_006717630.2:c.3857C= XP_006717693.1:p.Pro1286=
NM_000392.5:c.4553C= MANE Select NP_000383.2:p.Pro1518=
XM_006717630.3:c.3857C= XP_006717693.1:p.Pro1286=