Canonical Allele Identifier: CA1931511789
Gene: ABCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99844288_99844289delinsAT , CM000672.2:g.99844288_99844289delinsAT GRCh38
NC_000010.10:g.101604045_101604046delinsAT , CM000672.1:g.101604045_101604046delinsAT GRCh37
NC_000010.9:g.101594035_101594036delinsAT NCBI36
NG_011798.1:g.66583_66584delinsAT
NG_011798.2:g.66691_66692delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.3844-34_3844-33delinsAT MANE Select ENSP00000497274.1:n.3844-34_3844-33delinsAT
ENST00000649459.1:n.192-34_192-33delinsAT
ENST00000370449.8:c.3844-34_3844-33delinsAT ENSP00000359478.4:n.3844-34_3844-33delinsAT
NM_000392.4:c.3844-34_3844-33delinsAT NP_000383.1:n.3844-34_3844-33delinsAT
XM_006717630.2:c.3148-34_3148-33delinsAT XP_006717693.1:n.3148-34_3148-33delinsAT
XR_945604.1:n.4033-34_4033-33delinsAT
XR_945605.1:n.3908-34_3908-33delinsAT
NM_000392.5:c.3844-34_3844-33delinsAT MANE Select NP_000383.2:n.3844-34_3844-33delinsAT
XM_006717630.3:c.3148-34_3148-33delinsAT XP_006717693.1:n.3148-34_3148-33delinsAT
XR_945604.3:n.4087-34_4087-33delinsAT
XR_945605.3:n.3960-34_3960-33delinsAT