Canonical Allele Identifier: CA212845042

Gene: ABCC2

Linked Data

• dbSNP Id: rs111640918
• MyVariant Identifiers: chr10:g.101542496A>G (hg19) ; chr10:g.99782739A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99782739A>G , CM000672.2:g.99782739A>G	GRCh38
NC_000010.10:g.101542496A>G , CM000672.1:g.101542496A>G	GRCh37
NC_000010.9:g.101532486A>G	NCBI36
NG_011798.1:g.5034A>G
NG_011798.2:g.5142A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.-106A>G MANE Select	ENSP00000497274.1:n.-106A>G
ENST00000647836.1:n.100A>G
ENST00000648324.1:c.-106A>G	ENSP00000497248.1:n.-106A>G
ENST00000648689.1:c.-106A>G	ENSP00000496972.1:n.-106A>G
ENST00000649932.1:c.-106A>G	ENSP00000498120.1:n.-106A>G
ENST00000370449.8:c.-106A>G	ENSP00000359478.4:n.-106A>G
NM_000392.4:c.-106A>G	NP_000383.1:n.-106A>G
XM_006717631.2:c.-106A>G	XP_006717694.1:n.-106A>G
XM_011539291.1:c.-106A>G	XP_011537593.1:n.-106A>G
XR_945604.1:n.84A>G
XR_945605.1:n.86A>G
NM_000392.5:c.-106A>G MANE Select	NP_000383.2:n.-106A>G
XM_006717631.4:c.-106A>G	XP_006717694.1:n.-106A>G
XM_011539291.3:c.-106A>G	XP_011537593.1:n.-106A>G
XM_017015675.2:c.-106A>G	XP_016871164.1:n.-106A>G
XR_945604.3:n.138A>G
XR_945605.3:n.138A>G