Canonical Allele Identifier: CA368193638
Gene: SAMD9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.93104074A>G , CM000669.2:g.93104074A>G GRCh38
NC_000007.13:g.92733387A>G , CM000669.1:g.92733387A>G GRCh37
NC_000007.12:g.92571323A>G NCBI36
NG_023419.1:g.18950T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000379958.3:c.2024T>C MANE Select ENSP00000369292.2:p.Phe675Ser
ENST00000379958.2:c.2024T>C ENSP00000369292.2:p.Phe675Ser
ENST00000446617.1:c.2024T>C ENSP00000414529.1:p.Phe675Ser
ENST00000620985.4:c.2024T>C ENSP00000484636.1:p.Phe675Ser
NM_001193307.1:c.2024T>C NP_001180236.1:p.Phe675Ser
NM_017654.3:c.2024T>C NP_060124.2:p.Phe675Ser
NM_017654.4:c.2024T>C MANE Select NP_060124.2:p.Phe675Ser
NM_001193307.2:c.2024T>C NP_001180236.1:p.Phe675Ser