Canonical Allele Identifier: CA2555340206
Gene: ABCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99835932A>G , CM000672.2:g.99835932A>G GRCh38
NC_000010.10:g.101595689A>G , CM000672.1:g.101595689A>G GRCh37
NC_000010.9:g.101585679A>G NCBI36
NG_011798.1:g.58227A>G
NG_011798.2:g.58335A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.3415-159A>G MANE Select ENSP00000497274.1:n.3415-159A>G
ENST00000370449.8:c.3415-159A>G ENSP00000359478.4:n.3415-159A>G
NM_000392.4:c.3415-159A>G NP_000383.1:n.3415-159A>G
XM_006717630.2:c.2719-159A>G XP_006717693.1:n.2719-159A>G
XR_945604.1:n.3604-159A>G
XR_945605.1:n.3606-159A>G
NM_000392.5:c.3415-159A>G MANE Select NP_000383.2:n.3415-159A>G
XM_006717630.3:c.2719-159A>G XP_006717693.1:n.2719-159A>G
XR_945604.3:n.3658-159A>G
XR_945605.3:n.3658-159A>G