Canonical Allele Identifier: CA456624812
Gene: SAMD9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.92730743A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.93101430A>T , CM000669.2:g.93101430A>T GRCh38
NC_000007.13:g.92730743A>T , CM000669.1:g.92730743A>T GRCh37
NC_000007.12:g.92568679A>T NCBI36
NG_023419.1:g.21594T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000379958.3:c.4668T>A MANE Select ENSP00000369292.2:p.Ala1556=
ENST00000379958.2:c.4668T>A ENSP00000369292.2:p.Ala1556=
ENST00000620985.4:c.4668T>A ENSP00000484636.1:p.Ala1556=
NM_001193307.1:c.4668T>A NP_001180236.1:p.Ala1556=
NM_017654.3:c.4668T>A NP_060124.2:p.Ala1556=
NM_017654.4:c.4668T>A MANE Select NP_060124.2:p.Ala1556=
NM_001193307.2:c.4668T>A NP_001180236.1:p.Ala1556=