Canonical Allele Identifier: CA1931496504

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99836288C= , CM000672.2:g.99836288C=	GRCh38
NC_000010.10:g.101596045C= , CM000672.1:g.101596045C=	GRCh37
NC_000010.9:g.101586035C=	NCBI36
NG_011798.1:g.58583C=
NG_011798.2:g.58691C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3612C= MANE Select	ENSP00000497274.1:p.Asn1204=
ENST00000370449.8:c.3612C=	ENSP00000359478.4:p.Asn1204=
NM_000392.4:c.3612C=	NP_000383.1:p.Asn1204=
XM_006717630.2:c.2916C=	XP_006717693.1:p.Asn972=
XR_945604.1:n.3801C=
XR_945605.1:n.3803C=
NM_000392.5:c.3612C= MANE Select	NP_000383.2:p.Asn1204=
XM_006717630.3:c.2916C=	XP_006717693.1:p.Asn972=
XR_945604.3:n.3855C=
XR_945605.3:n.3855C=