Canonical Allele Identifier: CA471131374

Gene: ABCC2

Linked Data

• gnomAD v4: 10-99830410-C-T
• MyVariant Identifiers: chr10:g.101590167C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830410C>T , CM000672.2:g.99830410C>T	GRCh38
NC_000010.10:g.101590167C>T , CM000672.1:g.101590167C>T	GRCh37
NC_000010.9:g.101580157C>T	NCBI36
NG_011798.1:g.52705C>T
NG_011798.2:g.52813C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2724C>T MANE Select	ENSP00000497274.1:p.Ser908=
ENST00000370449.8:c.2724C>T	ENSP00000359478.4:p.Ser908=
NM_000392.4:c.2724C>T	NP_000383.1:p.Ser908=
XM_006717630.2:c.2028C>T	XP_006717693.1:p.Ser676=
XM_011539291.1:c.2724C>T	XP_011537593.1:p.Ser908=
XR_945604.1:n.2913C>T
XR_945605.1:n.2915C>T
NM_000392.5:c.2724C>T MANE Select	NP_000383.2:p.Ser908=
XM_006717630.3:c.2028C>T	XP_006717693.1:p.Ser676=
XM_011539291.3:c.2724C>T	XP_011537593.1:p.Ser908=
XR_945604.3:n.2967C>T
XR_945605.3:n.2967C>T