Canonical Allele Identifier: CA370691142
Community Standard Title: NM_000025.3(ADRB3):c.1066T>G (p.Phe356Val)
Gene: ADRB3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.37965404A>C , CM000670.2:g.37965404A>C GRCh38
NC_000008.10:g.37822922A>C , CM000670.1:g.37822922A>C GRCh37
NC_000008.9:g.37942079A>C NCBI36
NG_011936.1:g.6263T>G

Transcript Alleles

HGVS Amino-acid Change
NM_000025.3:c.1066T>G MANE Select NP_000016.1:p.Phe356Val
ENST00000345060.5:c.1066T>G MANE Select ENSP00000343782.3:p.Phe356Val
NM_000025.2:c.1066T>G NP_000016.1:p.Phe356Val
ENST00000345060.4:c.1066T>G ENSP00000343782.3:p.Phe356Val
ENST00000520341.1:n.341T>G
ENST00000520341.2:n.1194T>G
ENST00000614635.1:c.1066T>G ENSP00000480325.1:p.Phe356Val
ENST00000647937.1:c.550T>G ENSP00000497740.1:p.Phe184Val
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