Canonical Allele Identifier: CA378125208
Gene: ABCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99836277A>T , CM000672.2:g.99836277A>T GRCh38
NC_000010.10:g.101596034A>T , CM000672.1:g.101596034A>T GRCh37
NC_000010.9:g.101586024A>T NCBI36
NG_011798.1:g.58572A>T
NG_011798.2:g.58680A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.3601A>T MANE Select ENSP00000497274.1:p.Ile1201Phe
ENST00000370449.8:c.3601A>T ENSP00000359478.4:p.Ile1201Phe
NM_000392.4:c.3601A>T NP_000383.1:p.Ile1201Phe
XM_006717630.2:c.2905A>T XP_006717693.1:p.Ile969Phe
XR_945604.1:n.3790A>T
XR_945605.1:n.3792A>T
NM_000392.5:c.3601A>T MANE Select NP_000383.2:p.Ile1201Phe
XM_006717630.3:c.2905A>T XP_006717693.1:p.Ile969Phe
XR_945604.3:n.3844A>T
XR_945605.3:n.3844A>T