Canonical Allele Identifier: CA1931488829

Gene: ABCC2

Linked Data

• dbSNP Id: rs4148395

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830168G>T , CM000672.2:g.99830168G>T	GRCh38
NC_000010.10:g.101589925G>T , CM000672.1:g.101589925G>T	GRCh37
NC_000010.9:g.101579915G>T	NCBI36
NG_011798.1:g.52463G>T
NG_011798.2:g.52571G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.2621-139G>T MANE Select	ENSP00000497274.1:n.2621-139G>T
ENST00000370449.8:c.2621-139G>T	ENSP00000359478.4:n.2621-139G>T
NM_000392.4:c.2621-139G>T	NP_000383.1:n.2621-139G>T
XM_006717630.2:c.1925-139G>T	XP_006717693.1:n.1925-139G>T
XM_006717631.2:c.*48-139G>T	XP_006717694.1:n.*48-139G>T
XM_011539291.1:c.2621-139G>T	XP_011537593.1:n.2621-139G>T
XR_945604.1:n.2810-139G>T
XR_945605.1:n.2812-139G>T
NM_000392.5:c.2621-139G>T MANE Select	NP_000383.2:n.2621-139G>T
XM_006717630.3:c.1925-139G>T	XP_006717693.1:n.1925-139G>T
XM_006717631.4:c.*48-139G>T	XP_006717694.1:n.*48-139G>T
XM_011539291.3:c.2621-139G>T	XP_011537593.1:n.2621-139G>T
XR_945604.3:n.2864-139G>T
XR_945605.3:n.2864-139G>T