Canonical Allele Identifier: CA368192040
Gene: SAMD9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.93103870C>A , CM000669.2:g.93103870C>A GRCh38
NC_000007.13:g.92733183C>A , CM000669.1:g.92733183C>A GRCh37
NC_000007.12:g.92571119C>A NCBI36
NG_023419.1:g.19154G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000379958.3:c.2228G>T MANE Select ENSP00000369292.2:p.Gly743Val
ENST00000379958.2:c.2228G>T ENSP00000369292.2:p.Gly743Val
ENST00000446617.1:c.2228G>T ENSP00000414529.1:p.Gly743Val
ENST00000620985.4:c.2228G>T ENSP00000484636.1:p.Gly743Val
NM_001193307.1:c.2228G>T NP_001180236.1:p.Gly743Val
NM_017654.3:c.2228G>T NP_060124.2:p.Gly743Val
NM_017654.4:c.2228G>T MANE Select NP_060124.2:p.Gly743Val
NM_001193307.2:c.2228G>T NP_001180236.1:p.Gly743Val