Canonical Allele Identifier: CA1931496167
Gene: ABCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99836145_99836147delinsTCC , CM000672.2:g.99836145_99836147delinsTCC GRCh38
NC_000010.10:g.101595902_101595904delinsTCC , CM000672.1:g.101595902_101595904delinsTCC GRCh37
NC_000010.9:g.101585892_101585894delinsTCC NCBI36
NG_011798.1:g.58440_58442delinsTCC
NG_011798.2:g.58548_58550delinsTCC

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.3469_3471delinsTCC MANE Select ENSP00000497274.1:p.Ser1157=
ENST00000370449.8:c.3469_3471delinsTCC ENSP00000359478.4:p.Ser1157=
NM_000392.4:c.3469_3471delinsTCC NP_000383.1:p.Ser1157=
XM_006717630.2:c.2773_2775delinsTCC XP_006717693.1:p.Ser925=
XR_945604.1:n.3658_3660delinsTCC
XR_945605.1:n.3660_3662delinsTCC
NM_000392.5:c.3469_3471delinsTCC MANE Select NP_000383.2:p.Ser1157=
XM_006717630.3:c.2773_2775delinsTCC XP_006717693.1:p.Ser925=
XR_945604.3:n.3712_3714delinsTCC
XR_945605.3:n.3712_3714delinsTCC