Canonical Allele Identifier: CA471135699

Gene: ABCC2

Linked Data

• gnomAD v4: 10-99845770-C-T
• MyVariant Identifiers: chr10:g.101605527C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845770C>T , CM000672.2:g.99845770C>T	GRCh38
NC_000010.10:g.101605527C>T , CM000672.1:g.101605527C>T	GRCh37
NC_000010.9:g.101595517C>T	NCBI36
NG_011798.1:g.68065C>T
NG_011798.2:g.68173C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.4134C>T MANE Select	ENSP00000497274.1:p.Thr1378=
ENST00000648523.1:c.22C>T
ENST00000649459.1:n.482C>T
ENST00000370449.8:c.4134C>T	ENSP00000359478.4:p.Thr1378=
NM_000392.4:c.4134C>T	NP_000383.1:p.Thr1378=
XM_006717630.2:c.3438C>T	XP_006717693.1:p.Thr1146=
XR_945604.1:n.4264C>T
XR_945605.1:n.4198C>T
NM_000392.5:c.4134C>T MANE Select	NP_000383.2:p.Thr1378=
XM_006717630.3:c.3438C>T	XP_006717693.1:p.Thr1146=
XR_945604.3:n.4318C>T
XR_945605.3:n.4250C>T