Canonical Allele Identifier: CA368193499
Gene: SAMD9 HGNC NCBI

Linked Data

dbSNP Id: rs1791585756
gnomAD v3: 7-93104046-A-T
gnomAD v4: 7-93104046-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.93104046A>T , CM000669.2:g.93104046A>T GRCh38
NC_000007.13:g.92733359A>T , CM000669.1:g.92733359A>T GRCh37
NC_000007.12:g.92571295A>T NCBI36
NG_023419.1:g.18978T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000379958.3:c.2052T>A MANE Select ENSP00000369292.2:p.Tyr684Ter
ENST00000379958.2:c.2052T>A ENSP00000369292.2:p.Tyr684Ter
ENST00000446617.1:c.2052T>A ENSP00000414529.1:p.Tyr684Ter
ENST00000620985.4:c.2052T>A ENSP00000484636.1:p.Tyr684Ter
NM_001193307.1:c.2052T>A NP_001180236.1:p.Tyr684Ter
NM_017654.3:c.2052T>A NP_060124.2:p.Tyr684Ter
NM_017654.4:c.2052T>A MANE Select NP_060124.2:p.Tyr684Ter
NM_001193307.2:c.2052T>A NP_001180236.1:p.Tyr684Ter