Canonical Allele Identifier: CA212872839

Gene: ABCC2

Linked Data

• dbSNP Id: rs913500441
• gnomAD v4: 10-99851400-C-G
• MyVariant Identifiers: chr10:g.101611157C>G (hg19) ; chr10:g.99851400C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99851400C>G , CM000672.2:g.99851400C>G	GRCh38
NC_000010.10:g.101611157C>G , CM000672.1:g.101611157C>G	GRCh37
NC_000010.9:g.101601147C>G	NCBI36
NG_011798.1:g.73695C>G
NG_011798.2:g.73803C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.4509-102C>G MANE Select	ENSP00000497274.1:n.4509-102C>G
ENST00000648523.1:c.579-102C>G
ENST00000370449.8:c.4509-102C>G	ENSP00000359478.4:n.4509-102C>G
NM_000392.4:c.4509-102C>G	NP_000383.1:n.4509-102C>G
XM_006717630.2:c.3813-102C>G	XP_006717693.1:n.3813-102C>G
XR_945605.1:n.4573-102C>G
NM_000392.5:c.4509-102C>G MANE Select	NP_000383.2:n.4509-102C>G
XM_006717630.3:c.3813-102C>G	XP_006717693.1:n.3813-102C>G
XR_945605.3:n.4625-102C>G