Canonical Allele Identifier: CA471135594
Gene: ABCC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.101605443C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99845686C>T , CM000672.2:g.99845686C>T GRCh38
NC_000010.10:g.101605443C>T , CM000672.1:g.101605443C>T GRCh37
NC_000010.9:g.101595433C>T NCBI36
NG_011798.1:g.67981C>T
NG_011798.2:g.68089C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.4050C>T MANE Select ENSP00000497274.1:p.Ile1350=
ENST00000649459.1:n.398C>T
ENST00000370449.8:c.4050C>T ENSP00000359478.4:p.Ile1350=
NM_000392.4:c.4050C>T NP_000383.1:p.Ile1350=
XM_006717630.2:c.3354C>T XP_006717693.1:p.Ile1118=
XR_945604.1:n.4180C>T
XR_945605.1:n.4114C>T
NM_000392.5:c.4050C>T MANE Select NP_000383.2:p.Ile1350=
XM_006717630.3:c.3354C>T XP_006717693.1:p.Ile1118=
XR_945604.3:n.4234C>T
XR_945605.3:n.4166C>T