Canonical Allele Identifier: CA378120784

Gene: ABCC2

Linked Data

• gnomAD v4: 10-99830394-T-G
• MyVariant Identifiers: chr10:g.101590151T>G (hg19) ; chr10:g.99830394T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830394T>G , CM000672.2:g.99830394T>G	GRCh38
NC_000010.10:g.101590151T>G , CM000672.1:g.101590151T>G	GRCh37
NC_000010.9:g.101580141T>G	NCBI36
NG_011798.1:g.52689T>G
NG_011798.2:g.52797T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2708T>G MANE Select	ENSP00000497274.1:p.Met903Arg
ENST00000370449.8:c.2708T>G	ENSP00000359478.4:p.Met903Arg
NM_000392.4:c.2708T>G	NP_000383.1:p.Met903Arg
XM_006717630.2:c.2012T>G	XP_006717693.1:p.Met671Arg
XM_006717631.2:c.*135T>G	XP_006717694.1:n.*135T>G
XM_011539291.1:c.2708T>G	XP_011537593.1:p.Met903Arg
XR_945604.1:n.2897T>G
XR_945605.1:n.2899T>G
NM_000392.5:c.2708T>G MANE Select	NP_000383.2:p.Met903Arg
XM_006717630.3:c.2012T>G	XP_006717693.1:p.Met671Arg
XM_006717631.4:c.*135T>G	XP_006717694.1:n.*135T>G
XM_011539291.3:c.2708T>G	XP_011537593.1:p.Met903Arg
XR_945604.3:n.2951T>G
XR_945605.3:n.2951T>G