Canonical Allele Identifier: CA5643817

Gene: ABCC2

Linked Data

• dbSNP Id: rs746520129
• ExAC: 10:101595896 A / C
• gnomAD v2: 10-101595896-A-C
• gnomAD v4: 10-99836139-A-C
• MyVariant Identifiers: chr10:g.101595896A>C (hg19) ; chr10:g.99836139A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99836139A>C , CM000672.2:g.99836139A>C	GRCh38
NC_000010.10:g.101595896A>C , CM000672.1:g.101595896A>C	GRCh37
NC_000010.9:g.101585886A>C	NCBI36
NG_011798.1:g.58434A>C
NG_011798.2:g.58542A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.3463A>C MANE Select	ENSP00000497274.1:p.Thr1155Pro
ENST00000370449.8:c.3463A>C	ENSP00000359478.4:p.Thr1155Pro
NM_000392.4:c.3463A>C	NP_000383.1:p.Thr1155Pro
XM_006717630.2:c.2767A>C	XP_006717693.1:p.Thr923Pro
XR_945604.1:n.3652A>C
XR_945605.1:n.3654A>C
NM_000392.5:c.3463A>C MANE Select	NP_000383.2:p.Thr1155Pro
XM_006717630.3:c.2767A>C	XP_006717693.1:p.Thr923Pro
XR_945604.3:n.3706A>C
XR_945605.3:n.3706A>C