Canonical Allele Identifier: CA378124435
Gene: ABCC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.101595891C>A (hg19) chr10:g.99836134C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99836134C>A , CM000672.2:g.99836134C>A GRCh38
NC_000010.10:g.101595891C>A , CM000672.1:g.101595891C>A GRCh37
NC_000010.9:g.101585881C>A NCBI36
NG_011798.1:g.58429C>A
NG_011798.2:g.58537C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.3458C>A MANE Select ENSP00000497274.1:p.Ser1153Tyr
ENST00000370449.8:c.3458C>A ENSP00000359478.4:p.Ser1153Tyr
NM_000392.4:c.3458C>A NP_000383.1:p.Ser1153Tyr
XM_006717630.2:c.2762C>A XP_006717693.1:p.Ser921Tyr
XR_945604.1:n.3647C>A
XR_945605.1:n.3649C>A
NM_000392.5:c.3458C>A MANE Select NP_000383.2:p.Ser1153Tyr
XM_006717630.3:c.2762C>A XP_006717693.1:p.Ser921Tyr
XR_945604.3:n.3701C>A
XR_945605.3:n.3701C>A
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