Canonical Allele Identifier: CA471134146

Gene: ABCC2

Linked Data

• MyVariant Identifiers: chr10:g.101604172C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99844415C>T , CM000672.2:g.99844415C>T	GRCh38
NC_000010.10:g.101604172C>T , CM000672.1:g.101604172C>T	GRCh37
NC_000010.9:g.101594162C>T	NCBI36
NG_011798.1:g.66710C>T
NG_011798.2:g.66818C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3937C>T MANE Select	ENSP00000497274.1:p.Leu1313=
ENST00000649459.1:n.285C>T
ENST00000370449.8:c.3937C>T	ENSP00000359478.4:p.Leu1313=
NM_000392.4:c.3937C>T	NP_000383.1:p.Leu1313=
XM_006717630.2:c.3241C>T	XP_006717693.1:p.Leu1081=
XR_945604.1:n.4126C>T
XR_945605.1:n.4001C>T
NM_000392.5:c.3937C>T MANE Select	NP_000383.2:p.Leu1313=
XM_006717630.3:c.3241C>T	XP_006717693.1:p.Leu1081=
XR_945604.3:n.4180C>T
XR_945605.3:n.4053C>T