Canonical Allele Identifier: CA2610497697
Gene: ABCC2 HGNC NCBI

Linked Data

gnomAD v4: 10-99844252-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99844252A>G , CM000672.2:g.99844252A>G GRCh38
NC_000010.10:g.101604009A>G , CM000672.1:g.101604009A>G GRCh37
NC_000010.9:g.101593999A>G NCBI36
NG_011798.1:g.66547A>G
NG_011798.2:g.66655A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.3844-70A>G MANE Select ENSP00000497274.1:n.3844-70A>G
ENST00000649459.1:n.192-70A>G
ENST00000370449.8:c.3844-70A>G ENSP00000359478.4:n.3844-70A>G
NM_000392.4:c.3844-70A>G NP_000383.1:n.3844-70A>G
XM_006717630.2:c.3148-70A>G XP_006717693.1:n.3148-70A>G
XR_945604.1:n.4033-70A>G
XR_945605.1:n.3908-70A>G
NM_000392.5:c.3844-70A>G MANE Select NP_000383.2:n.3844-70A>G
XM_006717630.3:c.3148-70A>G XP_006717693.1:n.3148-70A>G
XR_945604.3:n.4087-70A>G
XR_945605.3:n.3960-70A>G
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