Canonical Allele Identifier: CA1931489017

Gene: ABCC2

Linked Data

• dbSNP Id: rs2038715182

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830303C>T , CM000672.2:g.99830303C>T	GRCh38
NC_000010.10:g.101590060C>T , CM000672.1:g.101590060C>T	GRCh37
NC_000010.9:g.101580050C>T	NCBI36
NG_011798.1:g.52598C>T
NG_011798.2:g.52706C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.2621-4C>T MANE Select	ENSP00000497274.1:n.2621-4C>T
ENST00000370449.8:c.2621-4C>T	ENSP00000359478.4:n.2621-4C>T
NM_000392.4:c.2621-4C>T	NP_000383.1:n.2621-4C>T
XM_006717630.2:c.1925-4C>T	XP_006717693.1:n.1925-4C>T
XM_006717631.2:c.*48-4C>T	XP_006717694.1:n.*48-4C>T
XM_011539291.1:c.2621-4C>T	XP_011537593.1:n.2621-4C>T
XR_945604.1:n.2810-4C>T
XR_945605.1:n.2812-4C>T
NM_000392.5:c.2621-4C>T MANE Select	NP_000383.2:n.2621-4C>T
XM_006717630.3:c.1925-4C>T	XP_006717693.1:n.1925-4C>T
XM_006717631.4:c.*48-4C>T	XP_006717694.1:n.*48-4C>T
XM_011539291.3:c.2621-4C>T	XP_011537593.1:n.2621-4C>T
XR_945604.3:n.2864-4C>T
XR_945605.3:n.2864-4C>T