Canonical Allele Identifier: CA1931446327

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99784690A= , CM000672.2:g.99784690A=	GRCh38
NC_000010.10:g.101544447A= , CM000672.1:g.101544447A=	GRCh37
NC_000010.9:g.101534437A=	NCBI36
NG_011798.2:g.7093A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000392.5:c.116A= MANE Select	NP_000383.2:p.Tyr39=
ENST00000647814.1:c.116A= MANE Select	ENSP00000497274.1:p.Tyr39=
ENST00000370434.1:c.116A=	ENSP00000359463.1:p.Tyr39=
ENST00000370449.8:c.116A=	ENSP00000359478.4:p.Tyr39=
ENST00000647836.1:n.321A=
ENST00000648324.1:c.116A=	ENSP00000497248.1:p.Tyr39=
ENST00000648689.1:c.116A=	ENSP00000496972.1:p.Tyr39=
ENST00000649493.1:c.116A=	ENSP00000496847.1:p.Tyr39=
ENST00000649932.1:c.116A=	ENSP00000498120.1:p.Tyr39=
XM_006717631.2:c.116A=	XP_006717694.1:p.Tyr39=
XM_006717631.4:c.116A=	XP_006717694.1:p.Tyr39=
XM_011539291.1:c.116A=	XP_011537593.1:p.Tyr39=
XM_011539291.3:c.116A=	XP_011537593.1:p.Tyr39=
XM_017015675.2:c.116A=	XP_016871164.1:p.Tyr39=
XR_945604.1:n.305A=
XR_945604.3:n.359A=
XR_945605.1:n.307A=
XR_945605.3:n.359A=