Canonical Allele Identifier: CA212842550

Gene: ABCC2

Linked Data

• dbSNP Id: rs758986395
• gnomAD v3: 10-99811537-C-A
• gnomAD v4: 10-99811537-C-A
• MyVariant Identifiers: chr10:g.101571294C>A (hg19) ; chr10:g.99811537C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99811537C>A , CM000672.2:g.99811537C>A	GRCh38
NC_000010.10:g.101571294C>A , CM000672.1:g.101571294C>A	GRCh37
NC_000010.9:g.101561284C>A	NCBI36
NG_011798.1:g.33832C>A
NG_011798.2:g.33940C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.1902C>A MANE Select	ENSP00000497274.1:p.Asp634Glu
ENST00000370449.8:c.1902C>A	ENSP00000359478.4:p.Asp634Glu
NM_000392.4:c.1902C>A	NP_000383.1:p.Asp634Glu
XM_006717630.2:c.1206C>A	XP_006717693.1:p.Asp402Glu
XM_006717631.2:c.1902C>A	XP_006717694.1:p.Asp634Glu
XM_011539291.1:c.1902C>A	XP_011537593.1:p.Asp634Glu
XR_945604.1:n.2091C>A
XR_945605.1:n.2093C>A
NM_000392.5:c.1902C>A MANE Select	NP_000383.2:p.Asp634Glu
XM_006717630.3:c.1206C>A	XP_006717693.1:p.Asp402Glu
XM_006717631.4:c.1902C>A	XP_006717694.1:p.Asp634Glu
XM_011539291.3:c.1902C>A	XP_011537593.1:p.Asp634Glu
XM_017015675.2:c.1902C>A	XP_016871164.1:p.Asp634Glu
XR_945604.3:n.2145C>A
XR_945605.3:n.2145C>A