Canonical Allele Identifier: CA471135501

Gene: ABCC2

Linked Data

• gnomAD v4: 10-99845665-C-T
• MyVariant Identifiers: chr10:g.101605422C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845665C>T , CM000672.2:g.99845665C>T	GRCh38
NC_000010.10:g.101605422C>T , CM000672.1:g.101605422C>T	GRCh37
NC_000010.9:g.101595412C>T	NCBI36
NG_011798.1:g.67960C>T
NG_011798.2:g.68068C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.4029C>T MANE Select	ENSP00000497274.1:p.Leu1343=
ENST00000649459.1:n.377C>T
ENST00000370449.8:c.4029C>T	ENSP00000359478.4:p.Leu1343=
NM_000392.4:c.4029C>T	NP_000383.1:p.Leu1343=
XM_006717630.2:c.3333C>T	XP_006717693.1:p.Leu1111=
XR_945604.1:n.4177-18C>T
XR_945605.1:n.4093C>T
NM_000392.5:c.4029C>T MANE Select	NP_000383.2:p.Leu1343=
XM_006717630.3:c.3333C>T	XP_006717693.1:p.Leu1111=
XR_945604.3:n.4231-18C>T
XR_945605.3:n.4145C>T