Canonical Allele Identifier: CA1777411822
Gene: STAR HGNC NCBI

Linked Data

dbSNP Id: rs1802580978
gnomAD v3: 8-38146773-A-G
gnomAD v4: 8-38146773-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38146773A>G , CM000670.2:g.38146773A>G GRCh38
NC_000008.10:g.38004291A>G , CM000670.1:g.38004291A>G GRCh37
NC_000008.9:g.38123448A>G NCBI36
NG_011827.1:g.9310T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000276449.9:c.307-326T>C MANE Select ENSP00000276449.3:n.307-326T>C
ENST00000276449.8:c.307-326T>C ENSP00000276449.3:n.307-326T>C
ENST00000520114.1:n.794-326T>C
ENST00000521236.1:c.61-326T>C ENSP00000430030.1:n.61-326T>C
ENST00000522050.1:c.243-326T>C
NM_000349.2:c.307-326T>C NP_000340.2:n.307-326T>C
XM_006716392.1:c.307-326T>C XP_006716455.1:n.307-326T>C
NM_000349.3:c.307-326T>C MANE Select NP_000340.2:n.307-326T>C
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