Canonical Allele Identifier: CA2610497661

Gene: ABCC2

Linked Data

• gnomAD v4: 10-99844193-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99844193A>T , CM000672.2:g.99844193A>T	GRCh38
NC_000010.10:g.101603950A>T , CM000672.1:g.101603950A>T	GRCh37
NC_000010.9:g.101593940A>T	NCBI36
NG_011798.1:g.66488A>T
NG_011798.2:g.66596A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3844-129A>T MANE Select	ENSP00000497274.1:n.3844-129A>T
ENST00000649459.1:n.192-129A>T
ENST00000370449.8:c.3844-129A>T	ENSP00000359478.4:n.3844-129A>T
NM_000392.4:c.3844-129A>T	NP_000383.1:n.3844-129A>T
XM_006717630.2:c.3148-129A>T	XP_006717693.1:n.3148-129A>T
XR_945604.1:n.4033-129A>T
XR_945605.1:n.3908-129A>T
NM_000392.5:c.3844-129A>T MANE Select	NP_000383.2:n.3844-129A>T
XM_006717630.3:c.3148-129A>T	XP_006717693.1:n.3148-129A>T
XR_945604.3:n.4087-129A>T
XR_945605.3:n.3960-129A>T