Canonical Allele Identifier: CA595453628

Gene: ABCC2

Linked Data

• dbSNP Id: rs1378276972
• gnomAD v2: 10-101604426-T-TG
• MyVariant Identifiers: chr10:g.101604426_101604427insG (hg19) ; chr10:g.99844669_99844670insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99844669_99844670insG , CM000672.2:g.99844669_99844670insG	GRCh38
NC_000010.10:g.101604426_101604427insG , CM000672.1:g.101604426_101604427insG	GRCh37
NC_000010.9:g.101594416_101594417insG	NCBI36
NG_011798.1:g.66964_66965insG
NG_011798.2:g.67072_67073insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3987+204_3987+205insG MANE Select	ENSP00000497274.1:n.3987+204_3987+205insG
ENST00000649459.1:n.335+204_335+205insG
ENST00000370449.8:c.3987+204_3987+205insG	ENSP00000359478.4:n.3987+204_3987+205insG
NM_000392.4:c.3987+204_3987+205insG	NP_000383.1:n.3987+204_3987+205insG
XM_006717630.2:c.3291+204_3291+205insG	XP_006717693.1:n.3291+204_3291+205insG
XR_945604.1:n.4176+204_4176+205insG
XR_945605.1:n.4051+204_4051+205insG
NM_000392.5:c.3987+204_3987+205insG MANE Select	NP_000383.2:n.3987+204_3987+205insG
XM_006717630.3:c.3291+204_3291+205insG	XP_006717693.1:n.3291+204_3291+205insG
XR_945604.3:n.4230+204_4230+205insG
XR_945605.3:n.4103+204_4103+205insG