Canonical Allele Identifier: CA1931511764
Gene: ABCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99844266T= , CM000672.2:g.99844266T= GRCh38
NC_000010.10:g.101604023T= , CM000672.1:g.101604023T= GRCh37
NC_000010.9:g.101594013T= NCBI36
NG_011798.1:g.66561T=
NG_011798.2:g.66669T=

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.3844-56T= MANE Select ENSP00000497274.1:n.3844-56T=
ENST00000649459.1:n.192-56T=
ENST00000370449.8:c.3844-56T= ENSP00000359478.4:n.3844-56T=
NM_000392.4:c.3844-56T= NP_000383.1:n.3844-56T=
XM_006717630.2:c.3148-56T= XP_006717693.1:n.3148-56T=
XR_945604.1:n.4033-56T=
XR_945605.1:n.3908-56T=
NM_000392.5:c.3844-56T= MANE Select NP_000383.2:n.3844-56T=
XM_006717630.3:c.3148-56T= XP_006717693.1:n.3148-56T=
XR_945604.3:n.4087-56T=
XR_945605.3:n.3960-56T=