Canonical Allele Identifier: CA5643441

Gene: ABCC2

Linked Data

• dbSNP Id: rs748562479
• ExAC: 10:101578551 T / C
• gnomAD v2: 10-101578551-T-C
• gnomAD v4: 10-99818794-T-C
• MyVariant Identifiers: chr10:g.101578551T>C (hg19) ; chr10:g.99818794T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99818794T>C , CM000672.2:g.99818794T>C	GRCh38
NC_000010.10:g.101578551T>C , CM000672.1:g.101578551T>C	GRCh37
NC_000010.9:g.101568541T>C	NCBI36
NG_011798.1:g.41089T>C
NG_011798.2:g.41197T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.2276T>C MANE Select	ENSP00000497274.1:p.Ile759Thr
ENST00000370449.8:c.2276T>C	ENSP00000359478.4:p.Ile759Thr
NM_000392.4:c.2276T>C	NP_000383.1:p.Ile759Thr
XM_006717630.2:c.1580T>C	XP_006717693.1:p.Ile527Thr
XM_006717631.2:c.2276T>C	XP_006717694.1:p.Ile759Thr
XM_011539291.1:c.2276T>C	XP_011537593.1:p.Ile759Thr
XR_945604.1:n.2465T>C
XR_945605.1:n.2467T>C
NM_000392.5:c.2276T>C MANE Select	NP_000383.2:p.Ile759Thr
XM_006717630.3:c.1580T>C	XP_006717693.1:p.Ile527Thr
XM_006717631.4:c.2276T>C	XP_006717694.1:p.Ile759Thr
XM_011539291.3:c.2276T>C	XP_011537593.1:p.Ile759Thr
XM_017015675.2:c.2276T>C	XP_016871164.1:p.Ile759Thr
XR_945604.3:n.2519T>C
XR_945605.3:n.2519T>C