Canonical Allele Identifier: CA5643558

Gene: ABCC2

Linked Data

• dbSNP Id: rs201874841
• ExAC: 10:101590157 G / T
• gnomAD v2: 10-101590157-G-T
• gnomAD v3: 10-99830400-G-T
• gnomAD v4: 10-99830400-G-T
• MyVariant Identifiers: chr10:g.101590157G>T (hg19) ; chr10:g.99830400G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830400G>T , CM000672.2:g.99830400G>T	GRCh38
NC_000010.10:g.101590157G>T , CM000672.1:g.101590157G>T	GRCh37
NC_000010.9:g.101580147G>T	NCBI36
NG_011798.1:g.52695G>T
NG_011798.2:g.52803G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2714G>T MANE Select	ENSP00000497274.1:p.Arg905Ile
ENST00000370449.8:c.2714G>T	ENSP00000359478.4:p.Arg905Ile
NM_000392.4:c.2714G>T	NP_000383.1:p.Arg905Ile
XM_006717630.2:c.2018G>T	XP_006717693.1:p.Arg673Ile
XM_011539291.1:c.2714G>T	XP_011537593.1:p.Arg905Ile
XR_945604.1:n.2903G>T
XR_945605.1:n.2905G>T
NM_000392.5:c.2714G>T MANE Select	NP_000383.2:p.Arg905Ile
XM_006717630.3:c.2018G>T	XP_006717693.1:p.Arg673Ile
XM_011539291.3:c.2714G>T	XP_011537593.1:p.Arg905Ile
XR_945604.3:n.2957G>T
XR_945605.3:n.2957G>T