Canonical Allele Identifier: CA2610497706

Gene: ABCC2

Linked Data

• gnomAD v4: 10-99844265-C-CACG

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99844265_99844266insACG , CM000672.2:g.99844265_99844266insACG	GRCh38
NC_000010.10:g.101604022_101604023insACG , CM000672.1:g.101604022_101604023insACG	GRCh37
NC_000010.9:g.101594012_101594013insACG	NCBI36
NG_011798.1:g.66560_66561insACG
NG_011798.2:g.66668_66669insACG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3844-57_3844-56insACG MANE Select	ENSP00000497274.1:n.3844-57_3844-56insACG
ENST00000649459.1:n.192-57_192-56insACG
ENST00000370449.8:c.3844-57_3844-56insACG	ENSP00000359478.4:n.3844-57_3844-56insACG
NM_000392.4:c.3844-57_3844-56insACG	NP_000383.1:n.3844-57_3844-56insACG
XM_006717630.2:c.3148-57_3148-56insACG	XP_006717693.1:n.3148-57_3148-56insACG
XR_945604.1:n.4033-57_4033-56insACG
XR_945605.1:n.3908-57_3908-56insACG
NM_000392.5:c.3844-57_3844-56insACG MANE Select	NP_000383.2:n.3844-57_3844-56insACG
XM_006717630.3:c.3148-57_3148-56insACG	XP_006717693.1:n.3148-57_3148-56insACG
XR_945604.3:n.4087-57_4087-56insACG
XR_945605.3:n.3960-57_3960-56insACG