Canonical Allele Identifier: CA378128060
Gene: ABCC2 HGNC NCBI

Linked Data

dbSNP Id: rs2039006007
MyVariant Identifiers: chr10:g.101605445T>A (hg19) chr10:g.99845688T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99845688T>A , CM000672.2:g.99845688T>A GRCh38
NC_000010.10:g.101605445T>A , CM000672.1:g.101605445T>A GRCh37
NC_000010.9:g.101595435T>A NCBI36
NG_011798.1:g.67983T>A
NG_011798.2:g.68091T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.4052T>A MANE Select ENSP00000497274.1:p.Leu1351Ter
ENST00000649459.1:n.400T>A
ENST00000370449.8:c.4052T>A ENSP00000359478.4:p.Leu1351Ter
NM_000392.4:c.4052T>A NP_000383.1:p.Leu1351Ter
XM_006717630.2:c.3356T>A XP_006717693.1:p.Leu1119Ter
XR_945604.1:n.4182T>A
XR_945605.1:n.4116T>A
NM_000392.5:c.4052T>A MANE Select NP_000383.2:p.Leu1351Ter
XM_006717630.3:c.3356T>A XP_006717693.1:p.Leu1119Ter
XR_945604.3:n.4236T>A
XR_945605.3:n.4168T>A
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