Canonical Allele Identifier: CA5644174

Gene: ABCC2

Linked Data

• dbSNP Id: rs773156504
• ExAC: 10:101611223 T / C
• gnomAD v2: 10-101611223-T-C
• gnomAD v4: 10-99851466-T-C
• MyVariant Identifiers: chr10:g.101611223T>C (hg19) ; chr10:g.99851466T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99851466T>C , CM000672.2:g.99851466T>C	GRCh38
NC_000010.10:g.101611223T>C , CM000672.1:g.101611223T>C	GRCh37
NC_000010.9:g.101601213T>C	NCBI36
NG_011798.1:g.73761T>C
NG_011798.2:g.73869T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.4509-36T>C MANE Select	ENSP00000497274.1:n.4509-36T>C
ENST00000648523.1:c.579-36T>C
ENST00000370449.8:c.4509-36T>C	ENSP00000359478.4:n.4509-36T>C
NM_000392.4:c.4509-36T>C	NP_000383.1:n.4509-36T>C
XM_006717630.2:c.3813-36T>C	XP_006717693.1:n.3813-36T>C
XR_945605.1:n.4573-36T>C
NM_000392.5:c.4509-36T>C MANE Select	NP_000383.2:n.4509-36T>C
XM_006717630.3:c.3813-36T>C	XP_006717693.1:n.3813-36T>C
XR_945605.3:n.4625-36T>C