Canonical Allele Identifier: CA1931511782
Gene: ABCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99844281C= , CM000672.2:g.99844281C= GRCh38
NC_000010.10:g.101604038C= , CM000672.1:g.101604038C= GRCh37
NC_000010.9:g.101594028C= NCBI36
NG_011798.1:g.66576C=
NG_011798.2:g.66684C=

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.3844-41C= MANE Select ENSP00000497274.1:n.3844-41C=
ENST00000649459.1:n.192-41C=
ENST00000370449.8:c.3844-41C= ENSP00000359478.4:n.3844-41C=
NM_000392.4:c.3844-41C= NP_000383.1:n.3844-41C=
XM_006717630.2:c.3148-41C= XP_006717693.1:n.3148-41C=
XR_945604.1:n.4033-41C=
XR_945605.1:n.3908-41C=
NM_000392.5:c.3844-41C= MANE Select NP_000383.2:n.3844-41C=
XM_006717630.3:c.3148-41C= XP_006717693.1:n.3148-41C=
XR_945604.3:n.4087-41C=
XR_945605.3:n.3960-41C=