Canonical Allele Identifier: CA2610497279

Gene: ABCC2

Linked Data

• gnomAD v4: 10-99836337-T-TTTTTTC

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99836337_99836338insTTTTTC , CM000672.2:g.99836337_99836338insTTTTTC	GRCh38
NC_000010.10:g.101596094_101596095insTTTTTC , CM000672.1:g.101596094_101596095insTTTTTC	GRCh37
NC_000010.9:g.101586084_101586085insTTTTTC	NCBI36
NG_011798.1:g.58632_58633insTTTTTC
NG_011798.2:g.58740_58741insTTTTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3614+47_3614+48insTTTTTC MANE Select	ENSP00000497274.1:n.3614+47_3614+48insTTTTTC
ENST00000370449.8:c.3614+47_3614+48insTTTTTC	ENSP00000359478.4:n.3614+47_3614+48insTTTTTC
NM_000392.4:c.3614+47_3614+48insTTTTTC	NP_000383.1:n.3614+47_3614+48insTTTTTC
XM_006717630.2:c.2918+47_2918+48insTTTTTC	XP_006717693.1:n.2918+47_2918+48insTTTTTC
XR_945604.1:n.3803+47_3803+48insTTTTTC
XR_945605.1:n.3805+47_3805+48insTTTTTC
NM_000392.5:c.3614+47_3614+48insTTTTTC MANE Select	NP_000383.2:n.3614+47_3614+48insTTTTTC
XM_006717630.3:c.2918+47_2918+48insTTTTTC	XP_006717693.1:n.2918+47_2918+48insTTTTTC
XR_945604.3:n.3857+47_3857+48insTTTTTC
XR_945605.3:n.3857+47_3857+48insTTTTTC