Canonical Allele Identifier: CA378128135
Gene: ABCC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.101605457G>C (hg19) chr10:g.99845700G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99845700G>C , CM000672.2:g.99845700G>C GRCh38
NC_000010.10:g.101605457G>C , CM000672.1:g.101605457G>C GRCh37
NC_000010.9:g.101595447G>C NCBI36
NG_011798.1:g.67995G>C
NG_011798.2:g.68103G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.4064G>C MANE Select ENSP00000497274.1:p.Gly1355Ala
ENST00000649459.1:n.412G>C
ENST00000370449.8:c.4064G>C ENSP00000359478.4:p.Gly1355Ala
NM_000392.4:c.4064G>C NP_000383.1:p.Gly1355Ala
XM_006717630.2:c.3368G>C XP_006717693.1:p.Gly1123Ala
XR_945604.1:n.4194G>C
XR_945605.1:n.4128G>C
NM_000392.5:c.4064G>C MANE Select NP_000383.2:p.Gly1355Ala
XM_006717630.3:c.3368G>C XP_006717693.1:p.Gly1123Ala
XR_945604.3:n.4248G>C
XR_945605.3:n.4180G>C
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