Canonical Allele Identifier: CA2574661856
Gene: ABCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99844264A>G , CM000672.2:g.99844264A>G GRCh38
NC_000010.10:g.101604021A>G , CM000672.1:g.101604021A>G GRCh37
NC_000010.9:g.101594011A>G NCBI36
NG_011798.1:g.66559A>G
NG_011798.2:g.66667A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.3844-58A>G MANE Select ENSP00000497274.1:n.3844-58A>G
ENST00000649459.1:n.192-58A>G
ENST00000370449.8:c.3844-58A>G ENSP00000359478.4:n.3844-58A>G
NM_000392.4:c.3844-58A>G NP_000383.1:n.3844-58A>G
XM_006717630.2:c.3148-58A>G XP_006717693.1:n.3148-58A>G
XR_945604.1:n.4033-58A>G
XR_945605.1:n.3908-58A>G
NM_000392.5:c.3844-58A>G MANE Select NP_000383.2:n.3844-58A>G
XM_006717630.3:c.3148-58A>G XP_006717693.1:n.3148-58A>G
XR_945604.3:n.4087-58A>G
XR_945605.3:n.3960-58A>G