Canonical Allele Identifier: CA378126700
Gene: ABCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99844353C>T , CM000672.2:g.99844353C>T GRCh38
NC_000010.10:g.101604110C>T , CM000672.1:g.101604110C>T GRCh37
NC_000010.9:g.101594100C>T NCBI36
NG_011798.1:g.66648C>T
NG_011798.2:g.66756C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.3875C>T MANE Select ENSP00000497274.1:p.Pro1292Leu
ENST00000649459.1:n.223C>T
ENST00000370449.8:c.3875C>T ENSP00000359478.4:p.Pro1292Leu
NM_000392.4:c.3875C>T NP_000383.1:p.Pro1292Leu
XM_006717630.2:c.3179C>T XP_006717693.1:p.Pro1060Leu
XR_945604.1:n.4064C>T
XR_945605.1:n.3939C>T
NM_000392.5:c.3875C>T MANE Select NP_000383.2:p.Pro1292Leu
XM_006717630.3:c.3179C>T XP_006717693.1:p.Pro1060Leu
XR_945604.3:n.4118C>T
XR_945605.3:n.3991C>T