Canonical Allele Identifier: CA5643822
Gene: ABCC2 HGNC NCBI

Linked Data

dbSNP Id: rs765042639

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99836153C>G , CM000672.2:g.99836153C>G GRCh38
NC_000010.10:g.101595910C>G , CM000672.1:g.101595910C>G GRCh37
NC_000010.9:g.101585900C>G NCBI36
NG_011798.1:g.58448C>G
NG_011798.2:g.58556C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.3477C>G MANE Select ENSP00000497274.1:p.Ile1159Met
ENST00000370449.8:c.3477C>G ENSP00000359478.4:p.Ile1159Met
NM_000392.4:c.3477C>G NP_000383.1:p.Ile1159Met
XM_006717630.2:c.2781C>G XP_006717693.1:p.Ile927Met
XR_945604.1:n.3666C>G
XR_945605.1:n.3668C>G
NM_000392.5:c.3477C>G MANE Select NP_000383.2:p.Ile1159Met
XM_006717630.3:c.2781C>G XP_006717693.1:p.Ile927Met
XR_945604.3:n.3720C>G
XR_945605.3:n.3720C>G