Canonical Allele Identifier: CA1931514238
Gene: ABCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99845804G= , CM000672.2:g.99845804G= GRCh38
NC_000010.10:g.101605561G= , CM000672.1:g.101605561G= GRCh37
NC_000010.9:g.101595551G= NCBI36
NG_011798.1:g.68099G=
NG_011798.2:g.68207G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.4146+22G= MANE Select ENSP00000497274.1:n.4146+22G=
ENST00000648523.1:c.34+22G=
ENST00000649459.1:n.494+22G=
ENST00000370449.8:c.4146+22G= ENSP00000359478.4:n.4146+22G=
NM_000392.4:c.4146+22G= NP_000383.1:n.4146+22G=
XM_006717630.2:c.3450+22G= XP_006717693.1:n.3450+22G=
XR_945604.1:n.4276+22G=
XR_945605.1:n.4210+22G=
NM_000392.5:c.4146+22G= MANE Select NP_000383.2:n.4146+22G=
XM_006717630.3:c.3450+22G= XP_006717693.1:n.3450+22G=
XR_945604.3:n.4330+22G=
XR_945605.3:n.4262+22G=