Canonical Allele Identifier: CA1931496201
Gene: ABCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99836151A= , CM000672.2:g.99836151A= GRCh38
NC_000010.10:g.101595908A= , CM000672.1:g.101595908A= GRCh37
NC_000010.9:g.101585898A= NCBI36
NG_011798.1:g.58446A=
NG_011798.2:g.58554A=

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.3475A= MANE Select ENSP00000497274.1:p.Ile1159=
ENST00000370449.8:c.3475A= ENSP00000359478.4:p.Ile1159=
NM_000392.4:c.3475A= NP_000383.1:p.Ile1159=
XM_006717630.2:c.2779A= XP_006717693.1:p.Ile927=
XR_945604.1:n.3664A=
XR_945605.1:n.3666A=
NM_000392.5:c.3475A= MANE Select NP_000383.2:p.Ile1159=
XM_006717630.3:c.2779A= XP_006717693.1:p.Ile927=
XR_945604.3:n.3718A=
XR_945605.3:n.3718A=