Canonical Allele Identifier: CA931736335

Gene: ABCC2

Linked Data

• dbSNP Id: rs2038809803
• gnomAD v3: 10-99835738-TTTCTC-T
• gnomAD v4: 10-99835738-TTTCTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99835740_99835744del , CM000672.2:g.99835740_99835744del	GRCh38
NC_000010.10:g.101595497_101595501del , CM000672.1:g.101595497_101595501del	GRCh37
NC_000010.9:g.101585487_101585491del	NCBI36
NG_011798.1:g.58035_58039del
NG_011798.2:g.58143_58147del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3415-351_3415-347del MANE Select	ENSP00000497274.1:n.3415-351_3415-347del
ENST00000370449.8:c.3415-351_3415-347del	ENSP00000359478.4:n.3415-351_3415-347del
NM_000392.4:c.3415-351_3415-347del	NP_000383.1:n.3415-351_3415-347del
XM_006717630.2:c.2719-351_2719-347del	XP_006717693.1:n.2719-351_2719-347del
XR_945604.1:n.3604-351_3604-347del
XR_945605.1:n.3606-351_3606-347del
NM_000392.5:c.3415-351_3415-347del MANE Select	NP_000383.2:n.3415-351_3415-347del
XM_006717630.3:c.2719-351_2719-347del	XP_006717693.1:n.2719-351_2719-347del
XR_945604.3:n.3658-351_3658-347del
XR_945605.3:n.3658-351_3658-347del