Canonical Allele Identifier: CA1931496349
Gene: ABCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99836217_99836239delinsCGATTTCTGAAACACAATGAGGT , CM000672.2:g.99836217_99836239delinsCGATTTCTGAAACACAATGAGGT GRCh38
NC_000010.10:g.101595974_101595996delinsCGATTTCTGAAACACAATGAGGT , CM000672.1:g.101595974_101595996delinsCGATTTCTGAAACACAATGAGGT GRCh37
NC_000010.9:g.101585964_101585986delinsCGATTTCTGAAACACAATGAGGT NCBI36
NG_011798.1:g.58512_58534delinsCGATTTCTGAAACACAATGAGGT
NG_011798.2:g.58620_58642delinsCGATTTCTGAAACACAATGAGGT

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.3541_3563delinsCGATTTCTGAAACACAATGAGGT MANE Select ENSP00000497274.1:p.Arg1181=
ENST00000370449.8:c.3541_3563delinsCGATTTCTGAAACACAATGAGGT ENSP00000359478.4:p.Arg1181=
NM_000392.4:c.3541_3563delinsCGATTTCTGAAACACAATGAGGT NP_000383.1:p.Arg1181=
XM_006717630.2:c.2845_2867delinsCGATTTCTGAAACACAATGAGGT XP_006717693.1:p.Arg949=
XR_945604.1:n.3730_3752delinsCGATTTCTGAAACACAATGAGGT
XR_945605.1:n.3732_3754delinsCGATTTCTGAAACACAATGAGGT
NM_000392.5:c.3541_3563delinsCGATTTCTGAAACACAATGAGGT MANE Select NP_000383.2:p.Arg1181=
XM_006717630.3:c.2845_2867delinsCGATTTCTGAAACACAATGAGGT XP_006717693.1:p.Arg949=
XR_945604.3:n.3784_3806delinsCGATTTCTGAAACACAATGAGGT
XR_945605.3:n.3784_3806delinsCGATTTCTGAAACACAATGAGGT