Canonical Allele Identifier: CA2610494618

Gene: ABCC2

Linked Data

• gnomAD v4: 10-99811615-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99811615C>A , CM000672.2:g.99811615C>A	GRCh38
NC_000010.10:g.101571372C>A , CM000672.1:g.101571372C>A	GRCh37
NC_000010.9:g.101561362C>A	NCBI36
NG_011798.1:g.33910C>A
NG_011798.2:g.34018C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.1967+13C>A MANE Select	ENSP00000497274.1:n.1967+13C>A
ENST00000370449.8:c.1967+13C>A	ENSP00000359478.4:n.1967+13C>A
NM_000392.4:c.1967+13C>A	NP_000383.1:n.1967+13C>A
XM_006717630.2:c.1271+13C>A	XP_006717693.1:n.1271+13C>A
XM_006717631.2:c.1967+13C>A	XP_006717694.1:n.1967+13C>A
XM_011539291.1:c.1967+13C>A	XP_011537593.1:n.1967+13C>A
XR_945604.1:n.2156+13C>A
XR_945605.1:n.2158+13C>A
NM_000392.5:c.1967+13C>A MANE Select	NP_000383.2:n.1967+13C>A
XM_006717630.3:c.1271+13C>A	XP_006717693.1:n.1271+13C>A
XM_006717631.4:c.1967+13C>A	XP_006717694.1:n.1967+13C>A
XM_011539291.3:c.1967+13C>A	XP_011537593.1:n.1967+13C>A
XM_017015675.2:c.1967+13C>A	XP_016871164.1:n.1967+13C>A
XR_945604.3:n.2210+13C>A
XR_945605.3:n.2210+13C>A