Canonical Allele Identifier: CA882232958
Gene: AKT2 HGNC NCBI

Linked Data

dbSNP Id: rs1309942025
MyVariant Identifiers: chr19:g.40791304C>A (hg19) chr19:g.40285397C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285397C>A , CM000681.2:g.40285397C>A GRCh38
NC_000019.9:g.40791304C>A , CM000681.1:g.40791304C>A GRCh37
NC_000019.8:g.45483144C>A NCBI36
NG_012038.2:g.4962G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000578123.5:c.-85+51G>T ENSP00000462022.1:n.-85+51G>T
XM_011526620.1:c.-85+51G>T XP_011524922.1:n.-85+51G>T
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