Canonical Allele Identifier: CA1931491971

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99811544A= , CM000672.2:g.99811544A=	GRCh38
NC_000010.10:g.101571301A= , CM000672.1:g.101571301A=	GRCh37
NC_000010.9:g.101561291A=	NCBI36
NG_011798.1:g.33839A=
NG_011798.2:g.33947A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.1909A= MANE Select	ENSP00000497274.1:p.Met637=
ENST00000370449.8:c.1909A=	ENSP00000359478.4:p.Met637=
NM_000392.4:c.1909A=	NP_000383.1:p.Met637=
XM_006717630.2:c.1213A=	XP_006717693.1:p.Met405=
XM_006717631.2:c.1909A=	XP_006717694.1:p.Met637=
XM_011539291.1:c.1909A=	XP_011537593.1:p.Met637=
XR_945604.1:n.2098A=
XR_945605.1:n.2100A=
NM_000392.5:c.1909A= MANE Select	NP_000383.2:p.Met637=
XM_006717630.3:c.1213A=	XP_006717693.1:p.Met405=
XM_006717631.4:c.1909A=	XP_006717694.1:p.Met637=
XM_011539291.3:c.1909A=	XP_011537593.1:p.Met637=
XM_017015675.2:c.1909A=	XP_016871164.1:p.Met637=
XR_945604.3:n.2152A=
XR_945605.3:n.2152A=