Canonical Allele Identifier: CA368177665
Gene: SAMD9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.92730843A>C (hg19) chr7:g.93101530A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.93101530A>C , CM000669.2:g.93101530A>C GRCh38
NC_000007.13:g.92730843A>C , CM000669.1:g.92730843A>C GRCh37
NC_000007.12:g.92568779A>C NCBI36
NG_023419.1:g.21494T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000379958.3:c.4568T>G MANE Select ENSP00000369292.2:p.Val1523Gly
ENST00000379958.2:c.4568T>G ENSP00000369292.2:p.Val1523Gly
ENST00000620985.4:c.4568T>G ENSP00000484636.1:p.Val1523Gly
NM_001193307.1:c.4568T>G NP_001180236.1:p.Val1523Gly
NM_017654.3:c.4568T>G NP_060124.2:p.Val1523Gly
NM_017654.4:c.4568T>G MANE Select NP_060124.2:p.Val1523Gly
NM_001193307.2:c.4568T>G NP_001180236.1:p.Val1523Gly
Search 100 bp 5'
Search 100 bp 3'