Canonical Allele Identifier: CA653547604

Gene: ABCC2

Linked Data

• COSMIC: COSN6955297

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99844504T>G , CM000672.2:g.99844504T>G	GRCh38
NC_000010.10:g.101604261T>G , CM000672.1:g.101604261T>G	GRCh37
NC_000010.9:g.101594251T>G	NCBI36
NG_011798.1:g.66799T>G
NG_011798.2:g.66907T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3987+39T>G MANE Select	ENSP00000497274.1:n.3987+39T>G
ENST00000649459.1:n.335+39T>G
ENST00000370449.8:c.3987+39T>G	ENSP00000359478.4:n.3987+39T>G
NM_000392.4:c.3987+39T>G	NP_000383.1:n.3987+39T>G
XM_006717630.2:c.3291+39T>G	XP_006717693.1:n.3291+39T>G
XR_945604.1:n.4176+39T>G
XR_945605.1:n.4051+39T>G
NM_000392.5:c.3987+39T>G MANE Select	NP_000383.2:n.3987+39T>G
XM_006717630.3:c.3291+39T>G	XP_006717693.1:n.3291+39T>G
XR_945604.3:n.4230+39T>G
XR_945605.3:n.4103+39T>G