Canonical Allele Identifier: CA670634190

Gene: ABCC2

Linked Data

• dbSNP Id: rs1312087996
• gnomAD v3: 10-99835818-TAGG-T
• gnomAD v4: 10-99835818-TAGG-T
• MyVariant Identifiers: chr10:g.101595576_101595578del (hg19) ; chr10:g.99835819_99835821del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99835822_99835824del , CM000672.2:g.99835822_99835824del	GRCh38
NC_000010.10:g.101595579_101595581del , CM000672.1:g.101595579_101595581del	GRCh37
NC_000010.9:g.101585569_101585571del	NCBI36
NG_011798.1:g.58117_58119del
NG_011798.2:g.58225_58227del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3415-269_3415-267del MANE Select	ENSP00000497274.1:n.3415-269_3415-267del
ENST00000370449.8:c.3415-269_3415-267del	ENSP00000359478.4:n.3415-269_3415-267del
NM_000392.4:c.3415-269_3415-267del	NP_000383.1:n.3415-269_3415-267del
XM_006717630.2:c.2719-269_2719-267del	XP_006717693.1:n.2719-269_2719-267del
XR_945604.1:n.3604-269_3604-267del
XR_945605.1:n.3606-269_3606-267del
NM_000392.5:c.3415-269_3415-267del MANE Select	NP_000383.2:n.3415-269_3415-267del
XM_006717630.3:c.2719-269_2719-267del	XP_006717693.1:n.2719-269_2719-267del
XR_945604.3:n.3658-269_3658-267del
XR_945605.3:n.3658-269_3658-267del