Canonical Allele Identifier: CA471131836
Gene: ABCC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.101595907A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99836150A>G , CM000672.2:g.99836150A>G GRCh38
NC_000010.10:g.101595907A>G , CM000672.1:g.101595907A>G GRCh37
NC_000010.9:g.101585897A>G NCBI36
NG_011798.1:g.58445A>G
NG_011798.2:g.58553A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.3474A>G MANE Select ENSP00000497274.1:p.Pro1158=
ENST00000370449.8:c.3474A>G ENSP00000359478.4:p.Pro1158=
NM_000392.4:c.3474A>G NP_000383.1:p.Pro1158=
XM_006717630.2:c.2778A>G XP_006717693.1:p.Pro926=
XR_945604.1:n.3663A>G
XR_945605.1:n.3665A>G
NM_000392.5:c.3474A>G MANE Select NP_000383.2:p.Pro1158=
XM_006717630.3:c.2778A>G XP_006717693.1:p.Pro926=
XR_945604.3:n.3717A>G
XR_945605.3:n.3717A>G