Canonical Allele Identifier: CA2610496327

Gene: ABCC2

Linked Data

• gnomAD v4: 10-99830489-TTTTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830493_99830496del , CM000672.2:g.99830493_99830496del	GRCh38
NC_000010.10:g.101590250_101590253del , CM000672.1:g.101590250_101590253del	GRCh37
NC_000010.9:g.101580240_101580243del	NCBI36
NG_011798.1:g.52788_52791del
NG_011798.2:g.52896_52899del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2747+60_2747+63del MANE Select	ENSP00000497274.1:n.2747+60_2747+63del
ENST00000370449.8:c.2747+60_2747+63del	ENSP00000359478.4:n.2747+60_2747+63del
NM_000392.4:c.2747+60_2747+63del	NP_000383.1:n.2747+60_2747+63del
XM_006717630.2:c.2051+60_2051+63del	XP_006717693.1:n.2051+60_2051+63del
XM_011539291.1:c.2747+60_2747+63del	XP_011537593.1:n.2747+60_2747+63del
XR_945604.1:n.2936+60_2936+63del
XR_945605.1:n.2938+60_2938+63del
NM_000392.5:c.2747+60_2747+63del MANE Select	NP_000383.2:n.2747+60_2747+63del
XM_006717630.3:c.2051+60_2051+63del	XP_006717693.1:n.2051+60_2051+63del
XM_011539291.3:c.2747+60_2747+63del	XP_011537593.1:n.2747+60_2747+63del
XR_945604.3:n.2990+60_2990+63del
XR_945605.3:n.2990+60_2990+63del