Canonical Allele Identifier: CA1931511596
Gene: ABCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99818791G= , CM000672.2:g.99818791G= GRCh38
NC_000010.10:g.101578548G= , CM000672.1:g.101578548G= GRCh37
NC_000010.9:g.101568538G= NCBI36
NG_011798.1:g.41086G=
NG_011798.2:g.41194G=

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.2273G= MANE Select ENSP00000497274.1:p.Gly758=
ENST00000370449.8:c.2273G= ENSP00000359478.4:p.Gly758=
NM_000392.4:c.2273G= NP_000383.1:p.Gly758=
XM_006717630.2:c.1577G= XP_006717693.1:p.Gly526=
XM_006717631.2:c.2273G= XP_006717694.1:p.Gly758=
XM_011539291.1:c.2273G= XP_011537593.1:p.Gly758=
XR_945604.1:n.2462G=
XR_945605.1:n.2464G=
NM_000392.5:c.2273G= MANE Select NP_000383.2:p.Gly758=
XM_006717630.3:c.1577G= XP_006717693.1:p.Gly526=
XM_006717631.4:c.2273G= XP_006717694.1:p.Gly758=
XM_011539291.3:c.2273G= XP_011537593.1:p.Gly758=
XM_017015675.2:c.2273G= XP_016871164.1:p.Gly758=
XR_945604.3:n.2516G=
XR_945605.3:n.2516G=