Canonical Allele Identifier: CA212857691

Gene: ABCC2

Linked Data

• dbSNP Id: rs1030505812
• gnomAD v4: 10-99830384-T-C
• MyVariant Identifiers: chr10:g.101590141T>C (hg19) ; chr10:g.99830384T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830384T>C , CM000672.2:g.99830384T>C	GRCh38
NC_000010.10:g.101590141T>C , CM000672.1:g.101590141T>C	GRCh37
NC_000010.9:g.101580131T>C	NCBI36
NG_011798.1:g.52679T>C
NG_011798.2:g.52787T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.2698T>C MANE Select	ENSP00000497274.1:p.Ser900Pro
ENST00000370449.8:c.2698T>C	ENSP00000359478.4:p.Ser900Pro
NM_000392.4:c.2698T>C	NP_000383.1:p.Ser900Pro
XM_006717630.2:c.2002T>C	XP_006717693.1:p.Ser668Pro
XM_006717631.2:c.*125T>C	XP_006717694.1:n.*125T>C
XM_011539291.1:c.2698T>C	XP_011537593.1:p.Ser900Pro
XR_945604.1:n.2887T>C
XR_945605.1:n.2889T>C
NM_000392.5:c.2698T>C MANE Select	NP_000383.2:p.Ser900Pro
XM_006717630.3:c.2002T>C	XP_006717693.1:p.Ser668Pro
XM_006717631.4:c.*125T>C	XP_006717694.1:n.*125T>C
XM_011539291.3:c.2698T>C	XP_011537593.1:p.Ser900Pro
XR_945604.3:n.2941T>C
XR_945605.3:n.2941T>C