Canonical Allele Identifier: CA1931484414
Gene: ABCC2 HGNC NCBI

Linked Data

dbSNP Id: rs2039086021
gnomAD v4: 10-99851378-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99851378A>G , CM000672.2:g.99851378A>G GRCh38
NC_000010.10:g.101611135A>G , CM000672.1:g.101611135A>G GRCh37
NC_000010.9:g.101601125A>G NCBI36
NG_011798.1:g.73673A>G
NG_011798.2:g.73781A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.4509-124A>G MANE Select ENSP00000497274.1:n.4509-124A>G
ENST00000648523.1:c.579-124A>G
ENST00000370449.8:c.4509-124A>G ENSP00000359478.4:n.4509-124A>G
NM_000392.4:c.4509-124A>G NP_000383.1:n.4509-124A>G
XM_006717630.2:c.3813-124A>G XP_006717693.1:n.3813-124A>G
XR_945605.1:n.4573-124A>G
NM_000392.5:c.4509-124A>G MANE Select NP_000383.2:n.4509-124A>G
XM_006717630.3:c.3813-124A>G XP_006717693.1:n.3813-124A>G
XR_945605.3:n.4625-124A>G
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