Canonical Allele Identifier: CA378124406

Gene: ABCC2

Linked Data

• dbSNP Id: rs769064396
• MyVariant Identifiers: chr10:g.101595884C>G (hg19) ; chr10:g.99836127C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99836127C>G , CM000672.2:g.99836127C>G	GRCh38
NC_000010.10:g.101595884C>G , CM000672.1:g.101595884C>G	GRCh37
NC_000010.9:g.101585874C>G	NCBI36
NG_011798.1:g.58422C>G
NG_011798.2:g.58530C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.3451C>G MANE Select	ENSP00000497274.1:p.Leu1151Val
ENST00000370449.8:c.3451C>G	ENSP00000359478.4:p.Leu1151Val
NM_000392.4:c.3451C>G	NP_000383.1:p.Leu1151Val
XM_006717630.2:c.2755C>G	XP_006717693.1:p.Leu919Val
XR_945604.1:n.3640C>G
XR_945605.1:n.3642C>G
NM_000392.5:c.3451C>G MANE Select	NP_000383.2:p.Leu1151Val
XM_006717630.3:c.2755C>G	XP_006717693.1:p.Leu919Val
XR_945604.3:n.3694C>G
XR_945605.3:n.3694C>G