Canonical Allele Identifier: CA456624904
Gene: SAMD9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.92730836T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.93101523T>C , CM000669.2:g.93101523T>C GRCh38
NC_000007.13:g.92730836T>C , CM000669.1:g.92730836T>C GRCh37
NC_000007.12:g.92568772T>C NCBI36
NG_023419.1:g.21501A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000379958.3:c.4575A>G MANE Select ENSP00000369292.2:p.Glu1525=
ENST00000379958.2:c.4575A>G ENSP00000369292.2:p.Glu1525=
ENST00000620985.4:c.4575A>G ENSP00000484636.1:p.Glu1525=
NM_001193307.1:c.4575A>G NP_001180236.1:p.Glu1525=
NM_017654.3:c.4575A>G NP_060124.2:p.Glu1525=
NM_017654.4:c.4575A>G MANE Select NP_060124.2:p.Glu1525=
NM_001193307.2:c.4575A>G NP_001180236.1:p.Glu1525=