Canonical Allele Identifier: CA1931511777
Gene: ABCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99844274T= , CM000672.2:g.99844274T= GRCh38
NC_000010.10:g.101604031T= , CM000672.1:g.101604031T= GRCh37
NC_000010.9:g.101594021T= NCBI36
NG_011798.1:g.66569T=
NG_011798.2:g.66677T=

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.3844-48T= MANE Select ENSP00000497274.1:n.3844-48T=
ENST00000649459.1:n.192-48T=
ENST00000370449.8:c.3844-48T= ENSP00000359478.4:n.3844-48T=
NM_000392.4:c.3844-48T= NP_000383.1:n.3844-48T=
XM_006717630.2:c.3148-48T= XP_006717693.1:n.3148-48T=
XR_945604.1:n.4033-48T=
XR_945605.1:n.3908-48T=
NM_000392.5:c.3844-48T= MANE Select NP_000383.2:n.3844-48T=
XM_006717630.3:c.3148-48T= XP_006717693.1:n.3148-48T=
XR_945604.3:n.4087-48T=
XR_945605.3:n.3960-48T=