Canonical Allele Identifier: CA2610498359
Gene: ABCC2 HGNC NCBI

Linked Data

gnomAD v4: 10-99851381-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99851381G>C , CM000672.2:g.99851381G>C GRCh38
NC_000010.10:g.101611138G>C , CM000672.1:g.101611138G>C GRCh37
NC_000010.9:g.101601128G>C NCBI36
NG_011798.1:g.73676G>C
NG_011798.2:g.73784G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.4509-121G>C MANE Select ENSP00000497274.1:n.4509-121G>C
ENST00000648523.1:c.579-121G>C
ENST00000370449.8:c.4509-121G>C ENSP00000359478.4:n.4509-121G>C
NM_000392.4:c.4509-121G>C NP_000383.1:n.4509-121G>C
XM_006717630.2:c.3813-121G>C XP_006717693.1:n.3813-121G>C
XR_945605.1:n.4573-121G>C
NM_000392.5:c.4509-121G>C MANE Select NP_000383.2:n.4509-121G>C
XM_006717630.3:c.3813-121G>C XP_006717693.1:n.3813-121G>C
XR_945605.3:n.4625-121G>C
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