Canonical Allele Identifier: CA471132062
Gene: ABCC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.101596003T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99836246T>A , CM000672.2:g.99836246T>A GRCh38
NC_000010.10:g.101596003T>A , CM000672.1:g.101596003T>A GRCh37
NC_000010.9:g.101585993T>A NCBI36
NG_011798.1:g.58541T>A
NG_011798.2:g.58649T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.3570T>A MANE Select ENSP00000497274.1:p.Ile1190=
ENST00000370449.8:c.3570T>A ENSP00000359478.4:p.Ile1190=
NM_000392.4:c.3570T>A NP_000383.1:p.Ile1190=
XM_006717630.2:c.2874T>A XP_006717693.1:p.Ile958=
XR_945604.1:n.3759T>A
XR_945605.1:n.3761T>A
NM_000392.5:c.3570T>A MANE Select NP_000383.2:p.Ile1190=
XM_006717630.3:c.2874T>A XP_006717693.1:p.Ile958=
XR_945604.3:n.3813T>A
XR_945605.3:n.3813T>A