Canonical Allele Identifier: CA368177713
Gene: SAMD9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.92730846T>A (hg19) chr7:g.93101533T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.93101533T>A , CM000669.2:g.93101533T>A GRCh38
NC_000007.13:g.92730846T>A , CM000669.1:g.92730846T>A GRCh37
NC_000007.12:g.92568782T>A NCBI36
NG_023419.1:g.21491A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000379958.3:c.4565A>T MANE Select ENSP00000369292.2:p.Lys1522Ile
ENST00000379958.2:c.4565A>T ENSP00000369292.2:p.Lys1522Ile
ENST00000620985.4:c.4565A>T ENSP00000484636.1:p.Lys1522Ile
NM_001193307.1:c.4565A>T NP_001180236.1:p.Lys1522Ile
NM_017654.3:c.4565A>T NP_060124.2:p.Lys1522Ile
NM_017654.4:c.4565A>T MANE Select NP_060124.2:p.Lys1522Ile
NM_001193307.2:c.4565A>T NP_001180236.1:p.Lys1522Ile
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