Canonical Allele Identifier: CA2574638414

Gene: ABCC2

Linked Data

• gnomAD v4: 10-99830461-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830461T>G , CM000672.2:g.99830461T>G	GRCh38
NC_000010.10:g.101590218T>G , CM000672.1:g.101590218T>G	GRCh37
NC_000010.9:g.101580208T>G	NCBI36
NG_011798.1:g.52756T>G
NG_011798.2:g.52864T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2747+28T>G MANE Select	ENSP00000497274.1:n.2747+28T>G
ENST00000370449.8:c.2747+28T>G	ENSP00000359478.4:n.2747+28T>G
NM_000392.4:c.2747+28T>G	NP_000383.1:n.2747+28T>G
XM_006717630.2:c.2051+28T>G	XP_006717693.1:n.2051+28T>G
XM_011539291.1:c.2747+28T>G	XP_011537593.1:n.2747+28T>G
XR_945604.1:n.2936+28T>G
XR_945605.1:n.2938+28T>G
NM_000392.5:c.2747+28T>G MANE Select	NP_000383.2:n.2747+28T>G
XM_006717630.3:c.2051+28T>G	XP_006717693.1:n.2051+28T>G
XM_011539291.3:c.2747+28T>G	XP_011537593.1:n.2747+28T>G
XR_945604.3:n.2990+28T>G
XR_945605.3:n.2990+28T>G