Canonical Allele Identifier: CA212872835
Gene: ABCC2 HGNC NCBI

Linked Data

dbSNP Id: rs557533644
gnomAD v2: 10-101611139-A-AT
gnomAD v3: 10-99851382-A-AT
gnomAD v4: 10-99851382-A-AT
MyVariant Identifiers: chr10:g.101611139_101611140insT (hg19) chr10:g.99851382_99851383insT (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99851386dup , CM000672.2:g.99851386dup GRCh38
NC_000010.10:g.101611143dup , CM000672.1:g.101611143dup GRCh37
NC_000010.9:g.101601133dup NCBI36
NG_011798.1:g.73681dup
NG_011798.2:g.73789dup

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.4509-116dup MANE Select ENSP00000497274.1:n.4509-116dup
ENST00000648523.1:c.579-116dup
ENST00000370449.8:c.4509-116dup ENSP00000359478.4:n.4509-116dup
NM_000392.4:c.4509-116dup NP_000383.1:n.4509-116dup
XM_006717630.2:c.3813-116dup XP_006717693.1:n.3813-116dup
XR_945605.1:n.4573-116dup
NM_000392.5:c.4509-116dup MANE Select NP_000383.2:n.4509-116dup
XM_006717630.3:c.3813-116dup XP_006717693.1:n.3813-116dup
XR_945605.3:n.4625-116dup
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