Canonical Allele Identifier: CA175091713
Gene: STAR HGNC NCBI

Linked Data

dbSNP Id: rs35728697
MyVariant Identifiers: chr8:g.38002652G>C (hg19) chr8:g.38145134G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38145134G>C , CM000670.2:g.38145134G>C GRCh38
NC_000008.10:g.38002652G>C , CM000670.1:g.38002652G>C GRCh37
NC_000008.9:g.38121809G>C NCBI36
NG_011827.1:g.10949C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000276449.9:c.744+88C>G MANE Select ENSP00000276449.3:n.744+88C>G
ENST00000276449.8:c.744+88C>G ENSP00000276449.3:n.744+88C>G
ENST00000520114.1:n.1966C>G
ENST00000522050.1:c.587-748C>G
NM_000349.2:c.744+88C>G NP_000340.2:n.744+88C>G
XM_006716392.1:c.651-748C>G XP_006716455.1:n.651-748C>G
NM_000349.3:c.744+88C>G MANE Select NP_000340.2:n.744+88C>G
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