Canonical Allele Identifier: CA368193871
Gene: SAMD9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.93104123C>T , CM000669.2:g.93104123C>T GRCh38
NC_000007.13:g.92733436C>T , CM000669.1:g.92733436C>T GRCh37
NC_000007.12:g.92571372C>T NCBI36
NG_023419.1:g.18901G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000379958.3:c.1975G>A MANE Select ENSP00000369292.2:p.Glu659Lys
ENST00000379958.2:c.1975G>A ENSP00000369292.2:p.Glu659Lys
ENST00000446617.1:c.1975G>A ENSP00000414529.1:p.Glu659Lys
ENST00000620985.4:c.1975G>A ENSP00000484636.1:p.Glu659Lys
NM_001193307.1:c.1975G>A NP_001180236.1:p.Glu659Lys
NM_017654.3:c.1975G>A NP_060124.2:p.Glu659Lys
NM_017654.4:c.1975G>A MANE Select NP_060124.2:p.Glu659Lys
NM_001193307.2:c.1975G>A NP_001180236.1:p.Glu659Lys