Canonical Allele Identifier: CA670630585

Gene: ABCC2

Linked Data

• dbSNP Id: rs1424306866
• MyVariant Identifiers: chr10:g.101590421_101590426del (hg19) ; chr10:g.99830664_99830669del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830665_99830670del , CM000672.2:g.99830665_99830670del	GRCh38
NC_000010.10:g.101590422_101590427del , CM000672.1:g.101590422_101590427del	GRCh37
NC_000010.9:g.101580412_101580417del	NCBI36
NG_011798.1:g.52960_52965del
NG_011798.2:g.53068_53073del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2748-51_2748-46del MANE Select	ENSP00000497274.1:n.2748-51_2748-46del
ENST00000370449.8:c.2748-51_2748-46del	ENSP00000359478.4:n.2748-51_2748-46del
NM_000392.4:c.2748-51_2748-46del	NP_000383.1:n.2748-51_2748-46del
XM_006717630.2:c.2052-51_2052-46del	XP_006717693.1:n.2052-51_2052-46del
XM_011539291.1:c.2747+232_2747+237del	XP_011537593.1:n.2747+232_2747+237del
XR_945604.1:n.2937-51_2937-46del
XR_945605.1:n.2939-51_2939-46del
NM_000392.5:c.2748-51_2748-46del MANE Select	NP_000383.2:n.2748-51_2748-46del
XM_006717630.3:c.2052-51_2052-46del	XP_006717693.1:n.2052-51_2052-46del
XM_011539291.3:c.2747+232_2747+237del	XP_011537593.1:n.2747+232_2747+237del
XR_945604.3:n.2991-51_2991-46del
XR_945605.3:n.2991-51_2991-46del