Canonical Allele Identifier: CA1931489689
Gene: ABCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99830658_99830659delinsGC , CM000672.2:g.99830658_99830659delinsGC GRCh38
NC_000010.10:g.101590415_101590416delinsGC , CM000672.1:g.101590415_101590416delinsGC GRCh37
NC_000010.9:g.101580405_101580406delinsGC NCBI36
NG_011798.1:g.52953_52954delinsGC
NG_011798.2:g.53061_53062delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.2748-58_2748-57delinsGC MANE Select ENSP00000497274.1:n.2748-58_2748-57delinsGC
ENST00000370449.8:c.2748-58_2748-57delinsGC ENSP00000359478.4:n.2748-58_2748-57delinsGC
NM_000392.4:c.2748-58_2748-57delinsGC NP_000383.1:n.2748-58_2748-57delinsGC
XM_006717630.2:c.2052-58_2052-57delinsGC XP_006717693.1:n.2052-58_2052-57delinsGC
XM_011539291.1:c.2747+225_2747+226delinsGC XP_011537593.1:n.2747+225_2747+226delinsGC
XR_945604.1:n.2937-58_2937-57delinsGC
XR_945605.1:n.2939-58_2939-57delinsGC
NM_000392.5:c.2748-58_2748-57delinsGC MANE Select NP_000383.2:n.2748-58_2748-57delinsGC
XM_006717630.3:c.2052-58_2052-57delinsGC XP_006717693.1:n.2052-58_2052-57delinsGC
XM_011539291.3:c.2747+225_2747+226delinsGC XP_011537593.1:n.2747+225_2747+226delinsGC
XR_945604.3:n.2991-58_2991-57delinsGC
XR_945605.3:n.2991-58_2991-57delinsGC