Canonical Allele Identifier: CA378128487
Gene: ABCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99845764G>C , CM000672.2:g.99845764G>C GRCh38
NC_000010.10:g.101605521G>C , CM000672.1:g.101605521G>C GRCh37
NC_000010.9:g.101595511G>C NCBI36
NG_011798.1:g.68059G>C
NG_011798.2:g.68167G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.4128G>C MANE Select ENSP00000497274.1:p.Lys1376Asn
ENST00000648523.1:c.16G>C
ENST00000649459.1:n.476G>C
ENST00000370449.8:c.4128G>C ENSP00000359478.4:p.Lys1376Asn
NM_000392.4:c.4128G>C NP_000383.1:p.Lys1376Asn
XM_006717630.2:c.3432G>C XP_006717693.1:p.Lys1144Asn
XR_945604.1:n.4258G>C
XR_945605.1:n.4192G>C
NM_000392.5:c.4128G>C MANE Select NP_000383.2:p.Lys1376Asn
XM_006717630.3:c.3432G>C XP_006717693.1:p.Lys1144Asn
XR_945604.3:n.4312G>C
XR_945605.3:n.4244G>C