Canonical Allele Identifier: CA368192233
Gene: SAMD9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.93103898G>A , CM000669.2:g.93103898G>A GRCh38
NC_000007.13:g.92733211G>A , CM000669.1:g.92733211G>A GRCh37
NC_000007.12:g.92571147G>A NCBI36
NG_023419.1:g.19126C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000379958.3:c.2200C>T MANE Select ENSP00000369292.2:p.His734Tyr
ENST00000379958.2:c.2200C>T ENSP00000369292.2:p.His734Tyr
ENST00000446617.1:c.2200C>T ENSP00000414529.1:p.His734Tyr
ENST00000620985.4:c.2200C>T ENSP00000484636.1:p.His734Tyr
NM_001193307.1:c.2200C>T NP_001180236.1:p.His734Tyr
NM_017654.3:c.2200C>T NP_060124.2:p.His734Tyr
NM_017654.4:c.2200C>T MANE Select NP_060124.2:p.His734Tyr
NM_001193307.2:c.2200C>T NP_001180236.1:p.His734Tyr