Canonical Allele Identifier: CA378125087
Gene: ABCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99836254A>G , CM000672.2:g.99836254A>G GRCh38
NC_000010.10:g.101596011A>G , CM000672.1:g.101596011A>G GRCh37
NC_000010.9:g.101586001A>G NCBI36
NG_011798.1:g.58549A>G
NG_011798.2:g.58657A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.3578A>G MANE Select ENSP00000497274.1:p.Asn1193Ser
ENST00000370449.8:c.3578A>G ENSP00000359478.4:p.Asn1193Ser
NM_000392.4:c.3578A>G NP_000383.1:p.Asn1193Ser
XM_006717630.2:c.2882A>G XP_006717693.1:p.Asn961Ser
XR_945604.1:n.3767A>G
XR_945605.1:n.3769A>G
NM_000392.5:c.3578A>G MANE Select NP_000383.2:p.Asn1193Ser
XM_006717630.3:c.2882A>G XP_006717693.1:p.Asn961Ser
XR_945604.3:n.3821A>G
XR_945605.3:n.3821A>G