Canonical Allele Identifier: CA471135639

Gene: ABCC2

Linked Data

• gnomAD v4: 10-99845728-T-C
• MyVariant Identifiers: chr10:g.101605485T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845728T>C , CM000672.2:g.99845728T>C	GRCh38
NC_000010.10:g.101605485T>C , CM000672.1:g.101605485T>C	GRCh37
NC_000010.9:g.101595475T>C	NCBI36
NG_011798.1:g.68023T>C
NG_011798.2:g.68131T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.4092T>C MANE Select	ENSP00000497274.1:p.Asp1364=
ENST00000649459.1:n.440T>C
ENST00000370449.8:c.4092T>C	ENSP00000359478.4:p.Asp1364=
NM_000392.4:c.4092T>C	NP_000383.1:p.Asp1364=
XM_006717630.2:c.3396T>C	XP_006717693.1:p.Asp1132=
XR_945604.1:n.4222T>C
XR_945605.1:n.4156T>C
NM_000392.5:c.4092T>C MANE Select	NP_000383.2:p.Asp1364=
XM_006717630.3:c.3396T>C	XP_006717693.1:p.Asp1132=
XR_945604.3:n.4276T>C
XR_945605.3:n.4208T>C