Canonical Allele Identifier: CA378124276
Gene: ABCC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.101595854T>A (hg19) chr10:g.99836097T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99836097T>A , CM000672.2:g.99836097T>A GRCh38
NC_000010.10:g.101595854T>A , CM000672.1:g.101595854T>A GRCh37
NC_000010.9:g.101585844T>A NCBI36
NG_011798.1:g.58392T>A
NG_011798.2:g.58500T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.3421T>A MANE Select ENSP00000497274.1:p.Tyr1141Asn
ENST00000370449.8:c.3421T>A ENSP00000359478.4:p.Tyr1141Asn
NM_000392.4:c.3421T>A NP_000383.1:p.Tyr1141Asn
XM_006717630.2:c.2725T>A XP_006717693.1:p.Tyr909Asn
XR_945604.1:n.3610T>A
XR_945605.1:n.3612T>A
NM_000392.5:c.3421T>A MANE Select NP_000383.2:p.Tyr1141Asn
XM_006717630.3:c.2725T>A XP_006717693.1:p.Tyr909Asn
XR_945604.3:n.3664T>A
XR_945605.3:n.3664T>A
Search 100 bp 5'
Search 100 bp 3'