Canonical Allele Identifier: CA1931513746
Gene: ABCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99845623G= , CM000672.2:g.99845623G= GRCh38
NC_000010.10:g.101605380G= , CM000672.1:g.101605380G= GRCh37
NC_000010.9:g.101595370G= NCBI36
NG_011798.1:g.67918G=
NG_011798.2:g.68026G=

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.3988-1G= MANE Select ENSP00000497274.1:n.3988-1G=
ENST00000649459.1:n.336-1G=
ENST00000370449.8:c.3988-1G= ENSP00000359478.4:n.3988-1G=
NM_000392.4:c.3988-1G= NP_000383.1:n.3988-1G=
XM_006717630.2:c.3292-1G= XP_006717693.1:n.3292-1G=
XR_945604.1:n.4177-60G=
XR_945605.1:n.4052-1G=
NM_000392.5:c.3988-1G= MANE Select NP_000383.2:n.3988-1G=
XM_006717630.3:c.3292-1G= XP_006717693.1:n.3292-1G=
XR_945604.3:n.4231-60G=
XR_945605.3:n.4104-1G=