Canonical Allele Identifier: CA471131380
Gene: ABCC2 HGNC NCBI

Linked Data

gnomAD v4: 10-99830416-T-C
MyVariant Identifiers: chr10:g.101590173T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99830416T>C , CM000672.2:g.99830416T>C GRCh38
NC_000010.10:g.101590173T>C , CM000672.1:g.101590173T>C GRCh37
NC_000010.9:g.101580163T>C NCBI36
NG_011798.1:g.52711T>C
NG_011798.2:g.52819T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.2730T>C MANE Select ENSP00000497274.1:p.Arg910=
ENST00000370449.8:c.2730T>C ENSP00000359478.4:p.Arg910=
NM_000392.4:c.2730T>C NP_000383.1:p.Arg910=
XM_006717630.2:c.2034T>C XP_006717693.1:p.Arg678=
XM_011539291.1:c.2730T>C XP_011537593.1:p.Arg910=
XR_945604.1:n.2919T>C
XR_945605.1:n.2921T>C
NM_000392.5:c.2730T>C MANE Select NP_000383.2:p.Arg910=
XM_006717630.3:c.2034T>C XP_006717693.1:p.Arg678=
XM_011539291.3:c.2730T>C XP_011537593.1:p.Arg910=
XR_945604.3:n.2973T>C
XR_945605.3:n.2973T>C
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