Canonical Allele Identifier: CA1931513556
Gene: ABCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99845530C= , CM000672.2:g.99845530C= GRCh38
NC_000010.10:g.101605287C= , CM000672.1:g.101605287C= GRCh37
NC_000010.9:g.101595277C= NCBI36
NG_011798.1:g.67825C=
NG_011798.2:g.67933C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.3988-94C= MANE Select ENSP00000497274.1:n.3988-94C=
ENST00000649459.1:n.336-94C=
ENST00000370449.8:c.3988-94C= ENSP00000359478.4:n.3988-94C=
NM_000392.4:c.3988-94C= NP_000383.1:n.3988-94C=
XM_006717630.2:c.3292-94C= XP_006717693.1:n.3292-94C=
XR_945604.1:n.4177-153C=
XR_945605.1:n.4052-94C=
NM_000392.5:c.3988-94C= MANE Select NP_000383.2:n.3988-94C=
XM_006717630.3:c.3292-94C= XP_006717693.1:n.3292-94C=
XR_945604.3:n.4231-153C=
XR_945605.3:n.4104-94C=