Canonical Allele Identifier: CA378128174

Gene: ABCC2

Linked Data

• MyVariant Identifiers: chr10:g.101605465A>C (hg19) ; chr10:g.99845708A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845708A>C , CM000672.2:g.99845708A>C	GRCh38
NC_000010.10:g.101605465A>C , CM000672.1:g.101605465A>C	GRCh37
NC_000010.9:g.101595455A>C	NCBI36
NG_011798.1:g.68003A>C
NG_011798.2:g.68111A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.4072A>C MANE Select	ENSP00000497274.1:p.Ile1358Leu
ENST00000649459.1:n.420A>C
ENST00000370449.8:c.4072A>C	ENSP00000359478.4:p.Ile1358Leu
NM_000392.4:c.4072A>C	NP_000383.1:p.Ile1358Leu
XM_006717630.2:c.3376A>C	XP_006717693.1:p.Ile1126Leu
XR_945604.1:n.4202A>C
XR_945605.1:n.4136A>C
NM_000392.5:c.4072A>C MANE Select	NP_000383.2:p.Ile1358Leu
XM_006717630.3:c.3376A>C	XP_006717693.1:p.Ile1126Leu
XR_945604.3:n.4256A>C
XR_945605.3:n.4188A>C