Canonical Allele Identifier: CA1931511451
Gene: ABCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99818692C= , CM000672.2:g.99818692C= GRCh38
NC_000010.10:g.101578449C= , CM000672.1:g.101578449C= GRCh37
NC_000010.9:g.101568439C= NCBI36
NG_011798.1:g.40987C=
NG_011798.2:g.41095C=

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.2272-98C= MANE Select ENSP00000497274.1:n.2272-98C=
ENST00000370449.8:c.2272-98C= ENSP00000359478.4:n.2272-98C=
NM_000392.4:c.2272-98C= NP_000383.1:n.2272-98C=
XM_006717630.2:c.1576-98C= XP_006717693.1:n.1576-98C=
XM_006717631.2:c.2272-98C= XP_006717694.1:n.2272-98C=
XM_011539291.1:c.2272-98C= XP_011537593.1:n.2272-98C=
XR_945604.1:n.2461-98C=
XR_945605.1:n.2463-98C=
NM_000392.5:c.2272-98C= MANE Select NP_000383.2:n.2272-98C=
XM_006717630.3:c.1576-98C= XP_006717693.1:n.1576-98C=
XM_006717631.4:c.2272-98C= XP_006717694.1:n.2272-98C=
XM_011539291.3:c.2272-98C= XP_011537593.1:n.2272-98C=
XM_017015675.2:c.2272-98C= XP_016871164.1:n.2272-98C=
XR_945604.3:n.2515-98C=
XR_945605.3:n.2515-98C=