Canonical Allele Identifier: CA368178573
Gene: SAMD9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.93101618G>C , CM000669.2:g.93101618G>C GRCh38
NC_000007.13:g.92730931G>C , CM000669.1:g.92730931G>C GRCh37
NC_000007.12:g.92568867G>C NCBI36
NG_023419.1:g.21406C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000379958.3:c.4480C>G MANE Select ENSP00000369292.2:p.His1494Asp
ENST00000379958.2:c.4480C>G ENSP00000369292.2:p.His1494Asp
ENST00000620985.4:c.4480C>G ENSP00000484636.1:p.His1494Asp
NM_001193307.1:c.4480C>G NP_001180236.1:p.His1494Asp
NM_017654.3:c.4480C>G NP_060124.2:p.His1494Asp
NM_017654.4:c.4480C>G MANE Select NP_060124.2:p.His1494Asp
NM_001193307.2:c.4480C>G NP_001180236.1:p.His1494Asp