Canonical Allele Identifier: CA370698672
Gene: STAR HGNC NCBI

Linked Data

dbSNP Id: rs1264956874
gnomAD v2: 8-38003483-G-C
gnomAD v4: 8-38145965-G-C
MyVariant Identifiers: chr8:g.38003483G>C (hg19) chr8:g.38145965G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38145965G>C , CM000670.2:g.38145965G>C GRCh38
NC_000008.10:g.38003483G>C , CM000670.1:g.38003483G>C GRCh37
NC_000008.9:g.38122640G>C NCBI36
NG_011827.1:g.10118C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000276449.9:c.648C>G MANE Select ENSP00000276449.3:p.Ile216Met
ENST00000276449.8:c.648C>G ENSP00000276449.3:p.Ile216Met
ENST00000520114.1:n.1135C>G
ENST00000522050.1:c.584C>G
NM_000349.2:c.648C>G NP_000340.2:p.Ile216Met
XM_006716392.1:c.648C>G XP_006716455.1:p.Ile216Met
NM_000349.3:c.648C>G MANE Select NP_000340.2:p.Ile216Met
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