Canonical Allele Identifier: CA212858461
Gene: ABCC2 HGNC NCBI

Linked Data

dbSNP Id: rs3740070

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99831661G>T , CM000672.2:g.99831661G>T GRCh38
NC_000010.10:g.101591418G>T , CM000672.1:g.101591418G>T GRCh37
NC_000010.9:g.101581408G>T NCBI36
NG_011798.1:g.53956G>T
NG_011798.2:g.54064G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.2934G>T MANE Select ENSP00000497274.1:p.Ser978=
ENST00000370449.8:c.2934G>T ENSP00000359478.4:p.Ser978=
NM_000392.4:c.2934G>T NP_000383.1:p.Ser978=
XM_006717630.2:c.2238G>T XP_006717693.1:p.Ser746=
XM_011539291.1:c.*47G>T XP_011537593.1:n.*47G>T
XR_945604.1:n.3123G>T
XR_945605.1:n.3125G>T
NM_000392.5:c.2934G>T MANE Select NP_000383.2:p.Ser978=
XM_006717630.3:c.2238G>T XP_006717693.1:p.Ser746=
XM_011539291.3:c.*47G>T XP_011537593.1:n.*47G>T
XR_945604.3:n.3177G>T
XR_945605.3:n.3177G>T