Canonical Allele Identifier: CA633110977
Gene: AKT2 HGNC NCBI

Linked Data

dbSNP Id: rs1600131843
gnomAD v2: 19-40791279-G-C
gnomAD v3: 19-40285372-G-C
gnomAD v4: 19-40285372-G-C
MyVariant Identifiers: chr19:g.40791279G>C (hg19) chr19:g.40285372G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285372G>C , CM000681.2:g.40285372G>C GRCh38
NC_000019.9:g.40791279G>C , CM000681.1:g.40791279G>C GRCh37
NC_000019.8:g.45483119G>C NCBI36
NG_012038.2:g.4987C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000391844.8:c.-322C>G ENSP00000375719.4:n.-322C>G
ENST00000392038.6:c.-276C>G ENSP00000375892.2:n.-276C>G
ENST00000424901.5:c.-276C>G ENSP00000399532.2:n.-276C>G
ENST00000578123.5:c.-85+76C>G ENSP00000462022.1:n.-85+76C>G
NM_001243027.2:c.-425C>G NP_001229956.1:n.-425C>G
NM_001243028.2:c.-332C>G NP_001229957.1:n.-332C>G
NM_001626.5:c.-276C>G NP_001617.1:n.-276C>G
XM_011526620.1:c.-85+76C>G XP_011524922.1:n.-85+76C>G
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