Canonical Allele Identifier: CA2610498362
Gene: ABCC2 HGNC NCBI

Linked Data

gnomAD v4: 10-99851388-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99851388A>T , CM000672.2:g.99851388A>T GRCh38
NC_000010.10:g.101611145A>T , CM000672.1:g.101611145A>T GRCh37
NC_000010.9:g.101601135A>T NCBI36
NG_011798.1:g.73683A>T
NG_011798.2:g.73791A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.4509-114A>T MANE Select ENSP00000497274.1:n.4509-114A>T
ENST00000648523.1:c.579-114A>T
ENST00000370449.8:c.4509-114A>T ENSP00000359478.4:n.4509-114A>T
NM_000392.4:c.4509-114A>T NP_000383.1:n.4509-114A>T
XM_006717630.2:c.3813-114A>T XP_006717693.1:n.3813-114A>T
XR_945605.1:n.4573-114A>T
NM_000392.5:c.4509-114A>T MANE Select NP_000383.2:n.4509-114A>T
XM_006717630.3:c.3813-114A>T XP_006717693.1:n.3813-114A>T
XR_945605.3:n.4625-114A>T
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