Canonical Allele Identifier: CA633111002
Gene: AKT2 HGNC NCBI

Linked Data

dbSNP Id: rs1411298267
gnomAD v2: 19-40791314-G-C
gnomAD v3: 19-40285407-G-C
gnomAD v4: 19-40285407-G-C
MyVariant Identifiers: chr19:g.40791314G>C (hg19) chr19:g.40285407G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285407G>C , CM000681.2:g.40285407G>C GRCh38
NC_000019.9:g.40791314G>C , CM000681.1:g.40791314G>C GRCh37
NC_000019.8:g.45483154G>C NCBI36
NG_012038.2:g.4952C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000578123.5:c.-85+41C>G ENSP00000462022.1:n.-85+41C>G
XM_011526620.1:c.-85+41C>G XP_011524922.1:n.-85+41C>G
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