Canonical Allele Identifier: CA368177726
Gene: SAMD9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.92730848T>G (hg19) chr7:g.93101535T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.93101535T>G , CM000669.2:g.93101535T>G GRCh38
NC_000007.13:g.92730848T>G , CM000669.1:g.92730848T>G GRCh37
NC_000007.12:g.92568784T>G NCBI36
NG_023419.1:g.21489A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000379958.3:c.4563A>C MANE Select ENSP00000369292.2:p.Glu1521Asp
ENST00000379958.2:c.4563A>C ENSP00000369292.2:p.Glu1521Asp
ENST00000620985.4:c.4563A>C ENSP00000484636.1:p.Glu1521Asp
NM_001193307.1:c.4563A>C NP_001180236.1:p.Glu1521Asp
NM_017654.3:c.4563A>C NP_060124.2:p.Glu1521Asp
NM_017654.4:c.4563A>C MANE Select NP_060124.2:p.Glu1521Asp
NM_001193307.2:c.4563A>C NP_001180236.1:p.Glu1521Asp
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