Canonical Allele Identifier: CA175095704
Gene: STAR HGNC NCBI

Linked Data

dbSNP Id: rs996610888
MyVariant Identifiers: chr8:g.38003444T>G (hg19) chr8:g.38145926T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38145926T>G , CM000670.2:g.38145926T>G GRCh38
NC_000008.10:g.38003444T>G , CM000670.1:g.38003444T>G GRCh37
NC_000008.9:g.38122601T>G NCBI36
NG_011827.1:g.10157A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000276449.9:c.650+37A>C MANE Select ENSP00000276449.3:n.650+37A>C
ENST00000276449.8:c.650+37A>C ENSP00000276449.3:n.650+37A>C
ENST00000520114.1:n.1174A>C
ENST00000522050.1:c.586+37A>C
NM_000349.2:c.650+37A>C NP_000340.2:n.650+37A>C
XM_006716392.1:c.650+37A>C XP_006716455.1:n.650+37A>C
NM_000349.3:c.650+37A>C MANE Select NP_000340.2:n.650+37A>C
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