Canonical Allele Identifier: CA2610497891
Gene: ABCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99845610A>T , CM000672.2:g.99845610A>T GRCh38
NC_000010.10:g.101605367A>T , CM000672.1:g.101605367A>T GRCh37
NC_000010.9:g.101595357A>T NCBI36
NG_011798.1:g.67905A>T
NG_011798.2:g.68013A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.3988-14A>T MANE Select ENSP00000497274.1:n.3988-14A>T
ENST00000649459.1:n.336-14A>T
ENST00000370449.8:c.3988-14A>T ENSP00000359478.4:n.3988-14A>T
NM_000392.4:c.3988-14A>T NP_000383.1:n.3988-14A>T
XM_006717630.2:c.3292-14A>T XP_006717693.1:n.3292-14A>T
XR_945604.1:n.4177-73A>T
XR_945605.1:n.4052-14A>T
NM_000392.5:c.3988-14A>T MANE Select NP_000383.2:n.3988-14A>T
XM_006717630.3:c.3292-14A>T XP_006717693.1:n.3292-14A>T
XR_945604.3:n.4231-73A>T
XR_945605.3:n.4104-14A>T