Canonical Allele Identifier: CA471135632

Gene: ABCC2

Linked Data

• MyVariant Identifiers: chr10:g.101605479A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845722A>C , CM000672.2:g.99845722A>C	GRCh38
NC_000010.10:g.101605479A>C , CM000672.1:g.101605479A>C	GRCh37
NC_000010.9:g.101595469A>C	NCBI36
NG_011798.1:g.68017A>C
NG_011798.2:g.68125A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.4086A>C MANE Select	ENSP00000497274.1:p.Gly1362=
ENST00000649459.1:n.434A>C
ENST00000370449.8:c.4086A>C	ENSP00000359478.4:p.Gly1362=
NM_000392.4:c.4086A>C	NP_000383.1:p.Gly1362=
XM_006717630.2:c.3390A>C	XP_006717693.1:p.Gly1130=
XR_945604.1:n.4216A>C
XR_945605.1:n.4150A>C
NM_000392.5:c.4086A>C MANE Select	NP_000383.2:p.Gly1362=
XM_006717630.3:c.3390A>C	XP_006717693.1:p.Gly1130=
XR_945604.3:n.4270A>C
XR_945605.3:n.4202A>C