Canonical Allele Identifier: CA471135616

Gene: ABCC2

Linked Data

• MyVariant Identifiers: chr10:g.101605455C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845698C>G , CM000672.2:g.99845698C>G	GRCh38
NC_000010.10:g.101605455C>G , CM000672.1:g.101605455C>G	GRCh37
NC_000010.9:g.101595445C>G	NCBI36
NG_011798.1:g.67993C>G
NG_011798.2:g.68101C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.4062C>G MANE Select	ENSP00000497274.1:p.Ala1354=
ENST00000649459.1:n.410C>G
ENST00000370449.8:c.4062C>G	ENSP00000359478.4:p.Ala1354=
NM_000392.4:c.4062C>G	NP_000383.1:p.Ala1354=
XM_006717630.2:c.3366C>G	XP_006717693.1:p.Ala1122=
XR_945604.1:n.4192C>G
XR_945605.1:n.4126C>G
NM_000392.5:c.4062C>G MANE Select	NP_000383.2:p.Ala1354=
XM_006717630.3:c.3366C>G	XP_006717693.1:p.Ala1122=
XR_945604.3:n.4246C>G
XR_945605.3:n.4178C>G