Canonical Allele Identifier: CA2610497195

Gene: ABCC2

Linked Data

• gnomAD v4: 10-99835953-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99835953G>T , CM000672.2:g.99835953G>T	GRCh38
NC_000010.10:g.101595710G>T , CM000672.1:g.101595710G>T	GRCh37
NC_000010.9:g.101585700G>T	NCBI36
NG_011798.1:g.58248G>T
NG_011798.2:g.58356G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3415-138G>T MANE Select	ENSP00000497274.1:n.3415-138G>T
ENST00000370449.8:c.3415-138G>T	ENSP00000359478.4:n.3415-138G>T
NM_000392.4:c.3415-138G>T	NP_000383.1:n.3415-138G>T
XM_006717630.2:c.2719-138G>T	XP_006717693.1:n.2719-138G>T
XR_945604.1:n.3604-138G>T
XR_945605.1:n.3606-138G>T
NM_000392.5:c.3415-138G>T MANE Select	NP_000383.2:n.3415-138G>T
XM_006717630.3:c.2719-138G>T	XP_006717693.1:n.2719-138G>T
XR_945604.3:n.3658-138G>T
XR_945605.3:n.3658-138G>T