Canonical Allele Identifier: CA5644026
Gene: ABCC2 HGNC NCBI

Linked Data

dbSNP Id: rs189165453
ExAC: 10:101605456 G / T
gnomAD v2: 10-101605456-G-T
gnomAD v3: 10-99845699-G-T
gnomAD v4: 10-99845699-G-T
MyVariant Identifiers: chr10:g.101605456G>T (hg19) chr10:g.99845699G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99845699G>T , CM000672.2:g.99845699G>T GRCh38
NC_000010.10:g.101605456G>T , CM000672.1:g.101605456G>T GRCh37
NC_000010.9:g.101595446G>T NCBI36
NG_011798.1:g.67994G>T
NG_011798.2:g.68102G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.4063G>T MANE Select ENSP00000497274.1:p.Gly1355Cys
ENST00000649459.1:n.411G>T
ENST00000370449.8:c.4063G>T ENSP00000359478.4:p.Gly1355Cys
NM_000392.4:c.4063G>T NP_000383.1:p.Gly1355Cys
XM_006717630.2:c.3367G>T XP_006717693.1:p.Gly1123Cys
XR_945604.1:n.4193G>T
XR_945605.1:n.4127G>T
NM_000392.5:c.4063G>T MANE Select NP_000383.2:p.Gly1355Cys
XM_006717630.3:c.3367G>T XP_006717693.1:p.Gly1123Cys
XR_945604.3:n.4247G>T
XR_945605.3:n.4179G>T
Search 100 bp 5'
Search 100 bp 3'