Canonical Allele Identifier: CA471131312

Gene: ABCC2

Linked Data

• gnomAD v4: 10-99830345-C-T
• MyVariant Identifiers: chr10:g.101590102C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830345C>T , CM000672.2:g.99830345C>T	GRCh38
NC_000010.10:g.101590102C>T , CM000672.1:g.101590102C>T	GRCh37
NC_000010.9:g.101580092C>T	NCBI36
NG_011798.1:g.52640C>T
NG_011798.2:g.52748C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2659C>T MANE Select	ENSP00000497274.1:p.Leu887=
ENST00000370449.8:c.2659C>T	ENSP00000359478.4:p.Leu887=
NM_000392.4:c.2659C>T	NP_000383.1:p.Leu887=
XM_006717630.2:c.1963C>T	XP_006717693.1:p.Leu655=
XM_006717631.2:c.*86C>T	XP_006717694.1:n.*86C>T
XM_011539291.1:c.2659C>T	XP_011537593.1:p.Leu887=
XR_945604.1:n.2848C>T
XR_945605.1:n.2850C>T
NM_000392.5:c.2659C>T MANE Select	NP_000383.2:p.Leu887=
XM_006717630.3:c.1963C>T	XP_006717693.1:p.Leu655=
XM_006717631.4:c.*86C>T	XP_006717694.1:n.*86C>T
XM_011539291.3:c.2659C>T	XP_011537593.1:p.Leu887=
XR_945604.3:n.2902C>T
XR_945605.3:n.2902C>T