Canonical Allele Identifier: CA5909523
Gene: SAA1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1059559

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18269742T>C , CM000673.2:g.18269742T>C GRCh38
NC_000011.9:g.18291289T>C , CM000673.1:g.18291289T>C GRCh37
NC_000011.8:g.18247865T>C NCBI36
NG_021330.1:g.8482T>C

Transcript Alleles

HGVS Amino-acid change
NM_000331.4:c.256T>C VV NP_000322.2:p.Phe86Leu
NM_001178006.1:c.256T>C VV NP_001171477.1:p.Phe86Leu
NM_199161.3:c.256T>C VV NP_954630.1:p.Phe86Leu
NM_000331.5:c.256T>C VV
NM_001178006.2:c.256T>C VV
NM_199161.4:c.256T>C VV
NM_199161.5:c.256T>C VV MANE Preferred NP_954630.2:p.Phe86Leu
ENST00000356524.8:c.256T>C ENSP00000348918.4:p.Phe86Leu
ENST00000405158.2:c.256T>C ENSP00000384906.2:p.Phe86Leu
ENST00000532858.5:c.256T>C ENSP00000436866.1:p.Phe86Leu