Canonical Allele Identifier: CA471131819

Gene: ABCC2

Linked Data

• MyVariant Identifiers: chr10:g.101595886G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99836129G>T , CM000672.2:g.99836129G>T	GRCh38
NC_000010.10:g.101595886G>T , CM000672.1:g.101595886G>T	GRCh37
NC_000010.9:g.101585876G>T	NCBI36
NG_011798.1:g.58424G>T
NG_011798.2:g.58532G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.3453G>T MANE Select	ENSP00000497274.1:p.Leu1151=
ENST00000370449.8:c.3453G>T	ENSP00000359478.4:p.Leu1151=
NM_000392.4:c.3453G>T	NP_000383.1:p.Leu1151=
XM_006717630.2:c.2757G>T	XP_006717693.1:p.Leu919=
XR_945604.1:n.3642G>T
XR_945605.1:n.3644G>T
NM_000392.5:c.3453G>T MANE Select	NP_000383.2:p.Leu1151=
XM_006717630.3:c.2757G>T	XP_006717693.1:p.Leu919=
XR_945604.3:n.3696G>T
XR_945605.3:n.3696G>T