Canonical Allele Identifier: CA471261779

Gene: ABCC2

Linked Data

• MyVariant Identifiers: chr10:g.101578552A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99818795A>C , CM000672.2:g.99818795A>C	GRCh38
NC_000010.10:g.101578552A>C , CM000672.1:g.101578552A>C	GRCh37
NC_000010.9:g.101568542A>C	NCBI36
NG_011798.1:g.41090A>C
NG_011798.2:g.41198A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.2277A>C MANE Select	ENSP00000497274.1:p.Ile759=
ENST00000370449.8:c.2277A>C	ENSP00000359478.4:p.Ile759=
NM_000392.4:c.2277A>C	NP_000383.1:p.Ile759=
XM_006717630.2:c.1581A>C	XP_006717693.1:p.Ile527=
XM_006717631.2:c.2277A>C	XP_006717694.1:p.Ile759=
XM_011539291.1:c.2277A>C	XP_011537593.1:p.Ile759=
XR_945604.1:n.2466A>C
XR_945605.1:n.2468A>C
NM_000392.5:c.2277A>C MANE Select	NP_000383.2:p.Ile759=
XM_006717630.3:c.1581A>C	XP_006717693.1:p.Ile527=
XM_006717631.4:c.2277A>C	XP_006717694.1:p.Ile759=
XM_011539291.3:c.2277A>C	XP_011537593.1:p.Ile759=
XM_017015675.2:c.2277A>C	XP_016871164.1:p.Ile759=
XR_945604.3:n.2520A>C
XR_945605.3:n.2520A>C