Canonical Allele Identifier: CA5643828
Gene: ABCC2 HGNC NCBI

Linked Data

dbSNP Id: rs767701081
ExAC: 10:101595928 G / T
gnomAD v2: 10-101595928-G-T
gnomAD v4: 10-99836171-G-T
MyVariant Identifiers: chr10:g.101595928G>T (hg19) chr10:g.99836171G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99836171G>T , CM000672.2:g.99836171G>T GRCh38
NC_000010.10:g.101595928G>T , CM000672.1:g.101595928G>T GRCh37
NC_000010.9:g.101585918G>T NCBI36
NG_011798.1:g.58466G>T
NG_011798.2:g.58574G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.3495G>T MANE Select ENSP00000497274.1:p.Glu1165Asp
ENST00000370449.8:c.3495G>T ENSP00000359478.4:p.Glu1165Asp
NM_000392.4:c.3495G>T NP_000383.1:p.Glu1165Asp
XM_006717630.2:c.2799G>T XP_006717693.1:p.Glu933Asp
XR_945604.1:n.3684G>T
XR_945605.1:n.3686G>T
NM_000392.5:c.3495G>T MANE Select NP_000383.2:p.Glu1165Asp
XM_006717630.3:c.2799G>T XP_006717693.1:p.Glu933Asp
XR_945604.3:n.3738G>T
XR_945605.3:n.3738G>T
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