Canonical Allele Identifier: CA378127141

Gene: ABCC2

Linked Data

• MyVariant Identifiers: chr10:g.101604134T>C (hg19) ; chr10:g.99844377T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99844377T>C , CM000672.2:g.99844377T>C	GRCh38
NC_000010.10:g.101604134T>C , CM000672.1:g.101604134T>C	GRCh37
NC_000010.9:g.101594124T>C	NCBI36
NG_011798.1:g.66672T>C
NG_011798.2:g.66780T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.3899T>C MANE Select	ENSP00000497274.1:p.Ile1300Thr
ENST00000649459.1:n.247T>C
ENST00000370449.8:c.3899T>C	ENSP00000359478.4:p.Ile1300Thr
NM_000392.4:c.3899T>C	NP_000383.1:p.Ile1300Thr
XM_006717630.2:c.3203T>C	XP_006717693.1:p.Ile1068Thr
XR_945604.1:n.4088T>C
XR_945605.1:n.3963T>C
NM_000392.5:c.3899T>C MANE Select	NP_000383.2:p.Ile1300Thr
XM_006717630.3:c.3203T>C	XP_006717693.1:p.Ile1068Thr
XR_945604.3:n.4142T>C
XR_945605.3:n.4015T>C