Canonical Allele Identifier: CA471131807

Gene: ABCC2

Linked Data

• dbSNP Id: rs2133124165
• MyVariant Identifiers: chr10:g.101595868C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99836111C>T , CM000672.2:g.99836111C>T	GRCh38
NC_000010.10:g.101595868C>T , CM000672.1:g.101595868C>T	GRCh37
NC_000010.9:g.101585858C>T	NCBI36
NG_011798.1:g.58406C>T
NG_011798.2:g.58514C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3435C>T MANE Select	ENSP00000497274.1:p.Ser1145=
ENST00000370449.8:c.3435C>T	ENSP00000359478.4:p.Ser1145=
NM_000392.4:c.3435C>T	NP_000383.1:p.Ser1145=
XM_006717630.2:c.2739C>T	XP_006717693.1:p.Ser913=
XR_945604.1:n.3624C>T
XR_945605.1:n.3626C>T
NM_000392.5:c.3435C>T MANE Select	NP_000383.2:p.Ser1145=
XM_006717630.3:c.2739C>T	XP_006717693.1:p.Ser913=
XR_945604.3:n.3678C>T
XR_945605.3:n.3678C>T