Canonical Allele Identifier: CA471131820
Gene: ABCC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.101595886G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99836129G>C , CM000672.2:g.99836129G>C GRCh38
NC_000010.10:g.101595886G>C , CM000672.1:g.101595886G>C GRCh37
NC_000010.9:g.101585876G>C NCBI36
NG_011798.1:g.58424G>C
NG_011798.2:g.58532G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.3453G>C MANE Select ENSP00000497274.1:p.Leu1151=
ENST00000370449.8:c.3453G>C ENSP00000359478.4:p.Leu1151=
NM_000392.4:c.3453G>C NP_000383.1:p.Leu1151=
XM_006717630.2:c.2757G>C XP_006717693.1:p.Leu919=
XR_945604.1:n.3642G>C
XR_945605.1:n.3644G>C
NM_000392.5:c.3453G>C MANE Select NP_000383.2:p.Leu1151=
XM_006717630.3:c.2757G>C XP_006717693.1:p.Leu919=
XR_945604.3:n.3696G>C
XR_945605.3:n.3696G>C
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