Canonical Allele Identifier: CA2686932338
Gene: STAR HGNC NCBI

Linked Data

gnomAD v4: 8-38145364-T-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38145364T>C , CM000670.2:g.38145364T>C GRCh38
NC_000008.10:g.38002882T>C , CM000670.1:g.38002882T>C GRCh37
NC_000008.9:g.38122039T>C NCBI36
NG_011827.1:g.10719A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000276449.9:c.651-49A>G MANE Select ENSP00000276449.3:n.651-49A>G
ENST00000276449.8:c.651-49A>G ENSP00000276449.3:n.651-49A>G
ENST00000520114.1:n.1736A>G
ENST00000522050.1:c.586+599A>G
NM_000349.2:c.651-49A>G NP_000340.2:n.651-49A>G
XM_006716392.1:c.650+599A>G XP_006716455.1:n.650+599A>G
NM_000349.3:c.651-49A>G MANE Select NP_000340.2:n.651-49A>G
Search 100 bp 5'
Search 100 bp 3'