Canonical Allele Identifier: CA1931513923
Gene: ABCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99845688T= , CM000672.2:g.99845688T= GRCh38
NC_000010.10:g.101605445T= , CM000672.1:g.101605445T= GRCh37
NC_000010.9:g.101595435T= NCBI36
NG_011798.1:g.67983T=
NG_011798.2:g.68091T=

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.4052T= MANE Select ENSP00000497274.1:p.Leu1351=
ENST00000649459.1:n.400T=
ENST00000370449.8:c.4052T= ENSP00000359478.4:p.Leu1351=
NM_000392.4:c.4052T= NP_000383.1:p.Leu1351=
XM_006717630.2:c.3356T= XP_006717693.1:p.Leu1119=
XR_945604.1:n.4182T=
XR_945605.1:n.4116T=
NM_000392.5:c.4052T= MANE Select NP_000383.2:p.Leu1351=
XM_006717630.3:c.3356T= XP_006717693.1:p.Leu1119=
XR_945604.3:n.4236T=
XR_945605.3:n.4168T=