Canonical Allele Identifier: CA5643862
Gene: ABCC2 HGNC NCBI

Linked Data

dbSNP Id: rs372032261
ExAC: 10:101596038 C / G
gnomAD v2: 10-101596038-C-G
gnomAD v3: 10-99836281-C-G
gnomAD v4: 10-99836281-C-G
MyVariant Identifiers: chr10:g.101596038C>G (hg19) chr10:g.99836281C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99836281C>G , CM000672.2:g.99836281C>G GRCh38
NC_000010.10:g.101596038C>G , CM000672.1:g.101596038C>G GRCh37
NC_000010.9:g.101586028C>G NCBI36
NG_011798.1:g.58576C>G
NG_011798.2:g.58684C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.3605C>G MANE Select ENSP00000497274.1:p.Thr1202Ser
ENST00000370449.8:c.3605C>G ENSP00000359478.4:p.Thr1202Ser
NM_000392.4:c.3605C>G NP_000383.1:p.Thr1202Ser
XM_006717630.2:c.2909C>G XP_006717693.1:p.Thr970Ser
XR_945604.1:n.3794C>G
XR_945605.1:n.3796C>G
NM_000392.5:c.3605C>G MANE Select NP_000383.2:p.Thr1202Ser
XM_006717630.3:c.2909C>G XP_006717693.1:p.Thr970Ser
XR_945604.3:n.3848C>G
XR_945605.3:n.3848C>G
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