Canonical Allele Identifier: CA1931511904
Gene: ABCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99844351G= , CM000672.2:g.99844351G= GRCh38
NC_000010.10:g.101604108G= , CM000672.1:g.101604108G= GRCh37
NC_000010.9:g.101594098G= NCBI36
NG_011798.1:g.66646G=
NG_011798.2:g.66754G=

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.3873G= MANE Select ENSP00000497274.1:p.Pro1291=
ENST00000649459.1:n.221G=
ENST00000370449.8:c.3873G= ENSP00000359478.4:p.Pro1291=
NM_000392.4:c.3873G= NP_000383.1:p.Pro1291=
XM_006717630.2:c.3177G= XP_006717693.1:p.Pro1059=
XR_945604.1:n.4062G=
XR_945605.1:n.3937G=
NM_000392.5:c.3873G= MANE Select NP_000383.2:p.Pro1291=
XM_006717630.3:c.3177G= XP_006717693.1:p.Pro1059=
XR_945604.3:n.4116G=
XR_945605.3:n.3989G=