Canonical Allele Identifier: CA378128137
Gene: ABCC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.101605459G>A (hg19) chr10:g.99845702G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99845702G>A , CM000672.2:g.99845702G>A GRCh38
NC_000010.10:g.101605459G>A , CM000672.1:g.101605459G>A GRCh37
NC_000010.9:g.101595449G>A NCBI36
NG_011798.1:g.67997G>A
NG_011798.2:g.68105G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.4066G>A MANE Select ENSP00000497274.1:p.Gly1356Ser
ENST00000649459.1:n.414G>A
ENST00000370449.8:c.4066G>A ENSP00000359478.4:p.Gly1356Ser
NM_000392.4:c.4066G>A NP_000383.1:p.Gly1356Ser
XM_006717630.2:c.3370G>A XP_006717693.1:p.Gly1124Ser
XR_945604.1:n.4196G>A
XR_945605.1:n.4130G>A
NM_000392.5:c.4066G>A MANE Select NP_000383.2:p.Gly1356Ser
XM_006717630.3:c.3370G>A XP_006717693.1:p.Gly1124Ser
XR_945604.3:n.4250G>A
XR_945605.3:n.4182G>A
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