Canonical Allele Identifier: CA670643613

Gene: ABCC2

Linked Data

• dbSNP Id: rs1243114055
• gnomAD v4: 10-99782747-A-G
• MyVariant Identifiers: chr10:g.101542504A>G (hg19) ; chr10:g.99782747A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99782747A>G , CM000672.2:g.99782747A>G	GRCh38
NC_000010.10:g.101542504A>G , CM000672.1:g.101542504A>G	GRCh37
NC_000010.9:g.101532494A>G	NCBI36
NG_011798.1:g.5042A>G
NG_011798.2:g.5150A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.-98A>G MANE Select	ENSP00000497274.1:n.-98A>G
ENST00000647836.1:n.108A>G
ENST00000648324.1:c.-98A>G	ENSP00000497248.1:n.-98A>G
ENST00000648689.1:c.-98A>G	ENSP00000496972.1:n.-98A>G
ENST00000649932.1:c.-98A>G	ENSP00000498120.1:n.-98A>G
ENST00000370449.8:c.-98A>G	ENSP00000359478.4:n.-98A>G
NM_000392.4:c.-98A>G	NP_000383.1:n.-98A>G
XM_006717631.2:c.-98A>G	XP_006717694.1:n.-98A>G
XM_011539291.1:c.-98A>G	XP_011537593.1:n.-98A>G
XR_945604.1:n.92A>G
XR_945605.1:n.94A>G
NM_000392.5:c.-98A>G MANE Select	NP_000383.2:n.-98A>G
XM_006717631.4:c.-98A>G	XP_006717694.1:n.-98A>G
XM_011539291.3:c.-98A>G	XP_011537593.1:n.-98A>G
XM_017015675.2:c.-98A>G	XP_016871164.1:n.-98A>G
XR_945604.3:n.146A>G
XR_945605.3:n.146A>G