Canonical Allele Identifier: CA368193529
Gene: SAMD9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.93104051A>C , CM000669.2:g.93104051A>C GRCh38
NC_000007.13:g.92733364A>C , CM000669.1:g.92733364A>C GRCh37
NC_000007.12:g.92571300A>C NCBI36
NG_023419.1:g.18973T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000379958.3:c.2047T>G MANE Select ENSP00000369292.2:p.Phe683Val
ENST00000379958.2:c.2047T>G ENSP00000369292.2:p.Phe683Val
ENST00000446617.1:c.2047T>G ENSP00000414529.1:p.Phe683Val
ENST00000620985.4:c.2047T>G ENSP00000484636.1:p.Phe683Val
NM_001193307.1:c.2047T>G NP_001180236.1:p.Phe683Val
NM_017654.3:c.2047T>G NP_060124.2:p.Phe683Val
NM_017654.4:c.2047T>G MANE Select NP_060124.2:p.Phe683Val
NM_001193307.2:c.2047T>G NP_001180236.1:p.Phe683Val