Canonical Allele Identifier: CA2739270970
Gene: ABCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2819852
ClinVar RCV Id: RCV003706478

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99811535_99811538del , CM000672.2:g.99811535_99811538del GRCh38
NC_000010.10:g.101571292_101571295del , CM000672.1:g.101571292_101571295del GRCh37
NC_000010.9:g.101561282_101561285del NCBI36
NG_011798.1:g.33830_33833del
NG_011798.2:g.33938_33941del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.1901-1_1903del
ENST00000370449.8:c.1901-1_1903del
NM_000392.4:c.1901-1_1903del
XM_006717630.2:c.1205-1_1207del
XM_006717631.2:c.1901-1_1903del
XM_011539291.1:c.1901-1_1903del
XR_945604.1:n.2090-1_2092del
XR_945605.1:n.2092-1_2094del
NM_000392.5:c.1901-1_1903del
XM_006717630.3:c.1205-1_1207del
XM_006717631.4:c.1901-1_1903del
XM_011539291.3:c.1901-1_1903del
XM_017015675.2:c.1901-1_1903del
XR_945604.3:n.2144-1_2146del
XR_945605.3:n.2144-1_2146del