Canonical Allele Identifier: CA378126634
Gene: ABCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99844322G>T , CM000672.2:g.99844322G>T GRCh38
NC_000010.10:g.101604079G>T , CM000672.1:g.101604079G>T GRCh37
NC_000010.9:g.101594069G>T NCBI36
NG_011798.1:g.66617G>T
NG_011798.2:g.66725G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.3844G>T MANE Select ENSP00000497274.1:p.Ala1282Ser
ENST00000649459.1:n.192G>T
ENST00000370449.8:c.3844G>T ENSP00000359478.4:p.Ala1282Ser
NM_000392.4:c.3844G>T NP_000383.1:p.Ala1282Ser
XM_006717630.2:c.3148G>T XP_006717693.1:p.Ala1050Ser
XR_945604.1:n.4033G>T
XR_945605.1:n.3908G>T
NM_000392.5:c.3844G>T MANE Select NP_000383.2:p.Ala1282Ser
XM_006717630.3:c.3148G>T XP_006717693.1:p.Ala1050Ser
XR_945604.3:n.4087G>T
XR_945605.3:n.3960G>T