Canonical Allele Identifier: CA595453624

Gene: ABCC2

Linked Data

• dbSNP Id: rs1244270878
• gnomAD v2: 10-101604414-T-TGTG
• MyVariant Identifiers: chr10:g.101604414_101604415insGTG (hg19) ; chr10:g.99844657_99844658insGTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99844657_99844658insGTG , CM000672.2:g.99844657_99844658insGTG	GRCh38
NC_000010.10:g.101604414_101604415insGTG , CM000672.1:g.101604414_101604415insGTG	GRCh37
NC_000010.9:g.101594404_101594405insGTG	NCBI36
NG_011798.1:g.66952_66953insGTG
NG_011798.2:g.67060_67061insGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3987+192_3987+193insGTG MANE Select	ENSP00000497274.1:n.3987+192_3987+193insGTG
ENST00000649459.1:n.335+192_335+193insGTG
ENST00000370449.8:c.3987+192_3987+193insGTG	ENSP00000359478.4:n.3987+192_3987+193insGTG
NM_000392.4:c.3987+192_3987+193insGTG	NP_000383.1:n.3987+192_3987+193insGTG
XM_006717630.2:c.3291+192_3291+193insGTG	XP_006717693.1:n.3291+192_3291+193insGTG
XR_945604.1:n.4176+192_4176+193insGTG
XR_945605.1:n.4051+192_4051+193insGTG
NM_000392.5:c.3987+192_3987+193insGTG MANE Select	NP_000383.2:n.3987+192_3987+193insGTG
XM_006717630.3:c.3291+192_3291+193insGTG	XP_006717693.1:n.3291+192_3291+193insGTG
XR_945604.3:n.4230+192_4230+193insGTG
XR_945605.3:n.4103+192_4103+193insGTG