Canonical Allele Identifier: CA175095637
Gene: STAR HGNC NCBI

Linked Data

dbSNP Id: rs934639676
gnomAD v3: 8-38145812-T-G
gnomAD v4: 8-38145812-T-G
MyVariant Identifiers: chr8:g.38003330T>G (hg19) chr8:g.38145812T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38145812T>G , CM000670.2:g.38145812T>G GRCh38
NC_000008.10:g.38003330T>G , CM000670.1:g.38003330T>G GRCh37
NC_000008.9:g.38122487T>G NCBI36
NG_011827.1:g.10271A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000276449.9:c.650+151A>C MANE Select ENSP00000276449.3:n.650+151A>C
ENST00000276449.8:c.650+151A>C ENSP00000276449.3:n.650+151A>C
ENST00000520114.1:n.1288A>C
ENST00000522050.1:c.586+151A>C
NM_000349.2:c.650+151A>C NP_000340.2:n.650+151A>C
XM_006716392.1:c.650+151A>C XP_006716455.1:n.650+151A>C
NM_000349.3:c.650+151A>C MANE Select NP_000340.2:n.650+151A>C
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