Canonical Allele Identifier: CA378126712
Gene: ABCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99844358T>G , CM000672.2:g.99844358T>G GRCh38
NC_000010.10:g.101604115T>G , CM000672.1:g.101604115T>G GRCh37
NC_000010.9:g.101594105T>G NCBI36
NG_011798.1:g.66653T>G
NG_011798.2:g.66761T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.3880T>G MANE Select ENSP00000497274.1:p.Trp1294Gly
ENST00000649459.1:n.228T>G
ENST00000370449.8:c.3880T>G ENSP00000359478.4:p.Trp1294Gly
NM_000392.4:c.3880T>G NP_000383.1:p.Trp1294Gly
XM_006717630.2:c.3184T>G XP_006717693.1:p.Trp1062Gly
XR_945604.1:n.4069T>G
XR_945605.1:n.3944T>G
NM_000392.5:c.3880T>G MANE Select NP_000383.2:p.Trp1294Gly
XM_006717630.3:c.3184T>G XP_006717693.1:p.Trp1062Gly
XR_945604.3:n.4123T>G
XR_945605.3:n.3996T>G