Canonical Allele Identifier: CA1931512342

Gene: ABCC2

Linked Data

• dbSNP Id: rs2038991708
• gnomAD v4: 10-99844617-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99844617A>T , CM000672.2:g.99844617A>T	GRCh38
NC_000010.10:g.101604374A>T , CM000672.1:g.101604374A>T	GRCh37
NC_000010.9:g.101594364A>T	NCBI36
NG_011798.1:g.66912A>T
NG_011798.2:g.67020A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3987+152A>T MANE Select	ENSP00000497274.1:n.3987+152A>T
ENST00000649459.1:n.335+152A>T
ENST00000370449.8:c.3987+152A>T	ENSP00000359478.4:n.3987+152A>T
NM_000392.4:c.3987+152A>T	NP_000383.1:n.3987+152A>T
XM_006717630.2:c.3291+152A>T	XP_006717693.1:n.3291+152A>T
XR_945604.1:n.4176+152A>T
XR_945605.1:n.4051+152A>T
NM_000392.5:c.3987+152A>T MANE Select	NP_000383.2:n.3987+152A>T
XM_006717630.3:c.3291+152A>T	XP_006717693.1:n.3291+152A>T
XR_945604.3:n.4230+152A>T
XR_945605.3:n.4103+152A>T